WebSuffolk Multispecialty Research (CBS) Sugar Lakes Family Practice Sugar Land, TX (Advarra) Summa Health (WIRB) Summit Headlands, LLC Portland, OR (Advarra) Summit Medical Group (WIRB) Summit Medical Group P.A. Learn how you can identify the signs of plantar fasciitis and find relief. Male and female subjects 60 years of age. Externships, Fellowships and Nurse Residency Programs, Perioperative Pre-Surgical, OR, PACU, Endoscopy. Healthy participants who are determined by medical history, physical examination (if required), and clinical judgment of the investigator to be eligible for inclusion in the study. This is a Phase 3, multicenter, randomized, double-blinded, placebo-controlled study to assess the safety, immunogenicity, and efficacy of RSVpreF or placebo (1:1 randomization) in adults. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. Individuals who receive treatment with radiotherapy or immunosuppressive therapy, including cytotoxic agents or systemic corticosteroids, eg, for cancer or an autoimmune disease, or planned receipt throughout the study. Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT05035212. Ability to comply with trial requirements, which necessitates access to transportation to on-site visits, including symptom visits for a nasopharyngeal swab. Clinically significant mental disorder that would prevent patients from giving informed consent and complying with study procedures (e.g., completion of the electronic diary). This was a promotional video for the hospital. Family medicine is a branch of primary care that acts in a generalist function to provide personal, front-line medical care to patients. Webparents are jealous of non parents The salaries of Nephrology Nurse Practitioners in New York City, NY range from $32,586 to $290,466 , with a median salary of $105,370 . Occurrence of complications and hospitalizations related to PCR-confirmed RSV disease. Call 646-929-7800 or Dr. Kerry McGregor, PsyD also suggests that some children express their gender identity as soon as they can talk. Talk with your doctor and family members or friends about deciding to join a study. Learn more about how to protect your child from a potentially harmful RSV infection. Talk with your doctor and family members or friends about deciding to join a study. (Clinical Trial), Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor), A PHASE 3, RANDOMIZED, OBSERVER-BLINDED STUDY TO EVALUATE THE EFFICACY, SAFETY, TOLERABILITY, AND IMMUNOGENICITY OF A MODIFIED RNA VACCINE AGAINST INFLUENZA COMPARED TO LICENSED INACTIVATED INFLUENZA VACCINE IN HEALTHY ADULTS 18 YEARS OF AGE OR OLDER, Experimental: Quadrivalent influenza modRNA vaccine, 18 through 64 years of age, Active Comparator: Quadrivalent influenza vaccine, 18 through 64 years of age, Experimental: Quadrivalent influenza modRNA vaccine, 65 years of age, Active Comparator: Quadrivalent influenza vaccine, 65 years of age, 18 Years and older (Adult, Older Adult), Birmingham, Alabama, United States, 35205, Accel Research Sites - Birmingham Clinical Research Unit, Birmingham, Alabama, United States, 35216, Huntsville, Alabama, United States, 35801, Fiel Family and Sports Medicine, PC/CCT Research, Anaheim, California, United States, 92801, Banning, California, United States, 92220, Fullerton, California, United States, 92835, Huntington Beach, California, United States, 92647, Velocity Clinical Research, Huntington Park, Huntington Park, California, United States, 90255, La Mesa, California, United States, 91942, Long Beach, California, United States, 90806, Los Angeles, California, United States, 90027, Los Angeles, California, United States, 90057, Velocity Clinical Research, North Hollywood, North Hollywood, California, United States, 91606, Paramount, California, United States, 90723, Redding, California, United States, 96001, Rolling Hills Estates, California, United States, 90274, Sacramento, California, United States, 95864, San Diego, California, United States, 92103, San Diego, California, United States, 92120, San Diego, California, United States, 92123, Spring Valley, California, United States, 91978, Toluca Lake, California, United States, 91602, Walnut Creek, California, United States, 94598, Fort Collins, Colorado, United States, 80525, Wheat Ridge, Colorado, United States, 80033, Bridgeport, Connecticut, United States, 06606, Milford, Connecticut, United States, 06460, New Haven, Connecticut, United States, 06511, New Haven, Connecticut, United States, 06519, Stamford, Connecticut, United States, 06905, Washington, District of Columbia, United States, 20017, Clearwater, Florida, United States, 33761, Alliance for Multispecialty Research, LLC, Coral Gables, Florida, United States, 33134, Fleming Island Center for Clinical Research, Fleming Island, Florida, United States, 32003, Fort Lauderdale, Florida, United States, 33308, Fort Myers, Florida, United States, 33912, Jacksonville Center for Clinical Research, Jacksonville, Florida, United States, 32216, Clinical Neuroscience Solutions, Inc. dba CNS Healthcare, Jacksonville, Florida, United States, 32256, Accel Research Sites - Lakeland Clinical Research Unit, Accel Research Sites - Maitland Clinical Research Unit, Miami Lakes, Florida, United States, 33016, Miami Dade Medical Research Institute, LLC, Palmetto Bay, Florida, United States, 33157, Pembroke Pines, Florida, United States, 33029, Accel Research Sites - St. Petersburg Clinical Research Unit, Saint Petersburg, Florida, United States, 33709, Clinical Site Partners LLC, dba CSP Orlando, Winter Park, Florida, United States, 32789, Sandy Springs, Georgia, United States, 30328, Stockbridge, Georgia, United States, 30281, SKY Clinical Research Network Group-Blake, Union City, Georgia, United States, 30291, Valparaiso, Indiana, United States, 46383, Lexington, Kentucky, United States, 40509, Versailles Family Medicine / CCT Research, Versailles, Kentucky, United States, 40383, New Orleans, Louisiana, United States, 70119, Louisiana State University Health Sciences Shreveport, Shreveport, Louisiana, United States, 71101, Baltimore, Maryland, United States, 21201, Silver Spring, Maryland, United States, 20904, Methuen, Massachusetts, United States, 01844, University of Massachusetts Chan Medical School, Worcester, Massachusetts, United States, 01655, Grosse Pointe Woods, Michigan, United States, 48236, Sterling Heights, Michigan, United States, 48312, Arcturus Healthcare , PLC, Troy Internal Medicine Research Division, Ridgeland, Mississippi, United States, 39157, Chesterfield, Missouri, United States, 63005, Saint Louis, Missouri, United States, 63141, Grand Island, Nebraska, United States, 68803, Papillion, Nebraska, United States, 68046, Portsmouth, New Hampshire, United States, 03801, Hackensack, New Jersey, United States, 07601, Hackensack University Medical Center Medical Plaza, Somers Point, New Jersey, United States, 08244, Albuquerque, New Mexico, United States, 87102, Horseheads, New York, United States, 14845, Rochester, New York, United States, 14609, Cary, North Carolina, United States, 27518, Charlotte, North Carolina, United States, 28209, Fayetteville, North Carolina, United States, 28303, Greensboro, North Carolina, United States, 27408, Hickory, North Carolina, United States, 28601, Raleigh, North Carolina, United States, 27609, Raleigh, North Carolina, United States, 27612, Rocky Mount, North Carolina, United States, 27804, Salisbury, North Carolina, United States, 28144, Wilmington, North Carolina, United States, 28401, Trial Management Associates - Wilmington - Floral Parkway, Wilmington, North Carolina, United States, 28403, Winston-Salem, North Carolina, United States, 27103, Fargo, North Dakota, United States, 58104, Cincinnati Children's Hospital Medical Center, University Hospitals Cleveland Medical Center, Oklahoma City, Oklahoma, United States, 73112, Camp Hill, Pennsylvania, United States, 17011, East Greenwich, Rhode Island, United States, 02818, Charleston, South Carolina, United States, 29412, Columbia, South Carolina, United States, 29204, Gaffney, South Carolina, United States, 29340, Greenville, South Carolina, United States, 29607, Little River, South Carolina, United States, 29566, Moncks Corner, South Carolina, United States, 29461, Myrtle Beach, South Carolina, United States, 29572, North Charleston, South Carolina, United States, 29405, Spartanburg, South Carolina, United States, 29303, Union, South Carolina, United States, 29379, Chattanooga, Tennessee, United States, 37421, Kingsport, Tennessee, United States, 37660, Knoxville, Tennessee, United States, 37909, North Texas Infectious Diseases Consultants, P.A, Invesclinic - Edinburg - West Trenton Road, Dynamed Clinical Research, LP d/b/a DM Clinical Research, South Ogden Family Medicine/ CCT Research, J. Lewis Research, Inc. / Foothill Family Clinic, Salt Lake City, Utah, United States, 84109, Salt Lake City, Utah, United States, 84117, J. Lewis Research, Inc. / Foothill Family Clinic South, Salt Lake City, Utah, United States, 84121, J. Lewis Research, Inc. / Jordan River Family Medicine, Springville Dermatology - Springville/CCT Research, Velocity Clinical Research, Salt Lake City, Clinical Alliance for Research and Education - Infectious Diseases (CARE-ID), LLC, Annandale, Virginia, United States, 22003, Charlottesville, Virginia, United States, 22911, Midlothian, Virginia, United States, 23114, Newport News, Virginia, United States, 23606, Portsmouth, Virginia, United States, 23703, Wauwatosa, Wisconsin, United States, 53226. Fever: greater than equal to (>=)38.0 degrees (deg) Celsius (C), mild (>=38.0 to 38.4 deg C, >38.4 to 38.9 deg C), moderate (>38.9 to 40.0 deg C and >40.0 deg C), severe (>38.9 deg C to 40.0 deg C) and grade 4 (>40.0 deg C). Listing a study does not mean it has been evaluated by the U.S. Federal Government. Any abnormal screening troponin I laboratory value. Medical or psychiatric condition, including recent (within the past year) or active suicidal ideation/behavior or laboratory abnormality, that may increase the risk of study participation or, in the investigator's judgment, make the participant inappropriate for the study. An NDCMC is defined as a disease or medical condition, not previously identified, that is expected to be persistent or otherwise long-lasting in its effects (eg, asthma). (Clinical Trial), Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor), SSA: observer-blinded, sponsor unblind SSB: single-blind, sponsor unblind, A PHASE 1/2 RANDOMIZED STUDY TO EVALUATE THE SAFETY, TOLERABILITY, AND IMMUNOGENICITY OF A MODIFIED RNA VACCINE AGAINST INFLUENZA IN HEALTHY INDIVIDUALS, Experimental: SSA: mIRV A (dose level 1) + QIV, Experimental: SSA: mIRV A (dose level 2) + QIV, Experimental: SSA: mIRV A (dose level 3) + QIV, Experimental: SSA: mIRV A (dose level 4) + QIV, Experimental: SSA: mIRV B (dose level 1) + QIV, Experimental: SSA: mIRV B (dose level 2) + QIV, Experimental: SSA: mIRV B (dose level 3) + QIV, Experimental: SSA: mIRV B (dose level 4) + QIV, Experimental: SSA: bIRV AB (dose level combination 1) + QIV, Experimental: SSA: bIRV AB (dose level combination 2) + QIV, Experimental: SSA: bIRV AB (dose level combination 3) + QIV, Experimental: SSA: bIRV AB (dose level combination 4) + QIV, Experimental: SSA: QIV + mIRV A strain (dose level 4), Experimental: SSA: qIRV (dose level 1) + QIV, Experimental: SSA: QIV + mIRV B strain (dose level 4), Experimental: SSB: 2 doses of qIRV (dose level 1), 2-visit schedule, Experimental: SSB: 2 doses of QIV, 2-visit schedule, Experimental: SSB: QIV + bIRV AA (dose level combination 1), 2-visit schedule, Experimental: SSB: QIV + bIRV AA (dose level combination 2), 2-visit schedule, Experimental: SSB: QIV + bIRV AA (dose level combination 1), 1-visit schedule, Experimental: SSB: QIV + bIRV AA (dose level combination 2), 1-visit schedule, Experimental: SSB: qIRV (dose level 2, dose combination 1), 1-visit schedule, Experimental: SSB: qIRV (dose level 2, dose combination 2), 1-visit schedule, Experimental: SSB: qIRV (dose level 3), 1-visit schedule, Experimental: SSB: bIRV AA + bIRV BB (both dose level combination 1), 1-visit schedule, Experimental: SSB: 1 dose of QIV, 1-visit schedule, Experimental: SSB: qIRV (dose level 1), 1-visit schedule, Experimental: SSB: qIRV (dose level 2), 1-visit schedule, 18 Years to 85 Years (Adult, Older Adult), Murrieta, California, United States, 92563, Riverside, California, United States, 92503, Pediatrics-Infectious Diseases - Clinical Trials Center at University of Colorado Anschutz Medical C, UCHealth Heart and Vascular Center - Anschutz Medical Campus, New Haven, Connecticut, United States, 06510, New Haven, Connecticut, United States, 06519, Alliance for Multispecialty Research, LLC, Coral Gables, Florida, United States, 33134, Daytona Beach, Florida, United States, 32114, Delray Beach, Florida, United States, 33484, Fleming Island, Florida, United States, 32003, Fleming Island Center for Clinical Research, Fort Lauderdale, Florida, United States, 33308, Fort Myers, Florida, United States, 33912, Jacksonville, Florida, United States, 32216, Clinical Neuroscience Solutions, Inc. dba CNS Healthcare, Jacksonville, Florida, United States, 32256, Premier Cardiology and Vascular Associates, Schiff Center for Liver Diseases/University of Miami, Miami Dade Medical Research Institute, LLC, Palmetto Bay, Florida, United States, 33157, Pembroke Pines, Florida, United States, 33029, Port Orange, Florida, United States, 32127, South Miami, Florida, United States, 33143, Winter Park, Florida, United States, 32789, Silver Spring, Maryland, United States, 20910, Meridian Clinical Research - 3345 North 107th Street, North Las Vegas, Nevada, United States, 89030, Somers Point, New Jersey, United States, 08244, NYU Langone - Center for the Prevention of Cardiovascular Disease, Rochester General Hospital Infectious Disease, Rochester, New York, United States, 14621, Rochester, New York, United States, 14642, Upstate Health Care Center-University Cardiovascular Group of Syracuse, SUNY Upstate Medical University Global Health Research Unit, Durham, North Carolina, United States, 27704, Fayetteville, North Carolina, United States, 28303, Monroe, North Carolina, United States, 28112, University Hospitals Cleveland Medical Center, Jenkintown, Pennsylvania, United States, 19046, Little River, South Carolina, United States, 29566. Northwell Health reserves the right to amend all terms of employment. Male participants able to father children must agree to use a highly effective method of contraception from the time of informed consent through at least 28 days after study intervention administration. Participants may be enrolled in either the reactogenicity subset, immunogenicity subset, or both subsets. Redness and swelling were measured and recorded in measuring device units. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. Inclusion Criteria: Male and female subjects 60 years of age. One injection, suspension for injection, intramuscular use, 0.5mL MVA-BN-RSV virus with a titer of at least 3 x 10E8 infectious units (Inf.U)/0.5mL in a Tris buffer at pH 7.7. Other medical or psychiatric condition including recent (within the past year) or active suicidal ideation/behavior or laboratory abnormality that may increase the risk of study participation or, in the investigator's judgment, make the participant inappropriate for the study. WebTidewater Physicians Multispecialty Group includes over 200 family medicine and specialty physicians, including advanced practice providers. Testing methods and laboratory result interpretation techniques are also studied extensively. Screening 12-lead ECG that, as judged by the investigator, is consistent with probable or possible myocarditis or pericarditis, or demonstrates clinically relevant abnormalities that may affect participant safety or interpretation of study results. WebThe Truly Awards celebrate the physicians of Northwell Health Physician Partners for the positive impact they make to change our lives. 1 measuring device unit =0.5 cm and graded as mild: 2.5 to 5.0 cm, moderate: > 5.0 to 10.0 cm and severe: >10 cm. Receipt of blood/plasma products, immunoglobulin, or monoclonal antibodies, from 60 days before study intervention administration, or planned receipt throughout the study. To obtain contact information for a study center near you, click here. - Vega Baja (WIRB), West Coast Research LLC Dublin, CA (Advarra), West Coast Retina Medical Group, Inc. (WIRB), West Houston Clinical Research Service Houston, TX (Advarra), West Houston Clinical Research Service, LLC (WIRB), West Michigan Clinical Research Center Wyoming, MI (Advarra), West Virginia Research Institute PLLC (WIRB), West Virginia School of Osteopathic Medicine, West Virginia University Eye Institute Morgantown, WV (Advarra), Western Carolina Retinal Associates P.A. We strive to make your visit as smooth as possible. Choosing to participate in a study is an important personal decision. Occurrence of any grade 3 or higher adverse events assessed as related to study vaccine within 29 days after vaccination. For participants 65 to 85 years of age at the time of enrollment, receipt of licensed influenza vaccination for the 2021-2022 northern hemisphere season >4 months (120 days) before study intervention administration. Please remove one or more studies before adding more. Absence of known, current, and life-limiting diagnoses that render survival to completion of the protocol unlikely. Clinica Privada Instituto Medico Platense S.A. La Plata, Buenos Aires, Argentina, B1900AVG, Instituto De Investigaciones Clnicas Mar Del Plata, Mar del Plata, Buenos Aires, Argentina, B7600FZO, Clinica Mayo de Urgencias Medicas Cruz Blanca S.R.L, San Miguel de Tucuman, Tucuman, Argentina, 4000, Hospital de Clinicas Presidente Nicolas Avellaneda, IMAC - Instituto Medico de Alta Complejidad, LMC Clinical Research Inc. (Clinical Pharmacology Unit), Dr. Anil K. Gupta Medicine Professional Corporation, Clinique de Mdecine Urbaine du Quartier Latin, St-Charles-Borromee, Quebec, Canada, J6E 2B4, Medical Corporation Heishinkai OPHAC Hospital, Medical Corp. Seikoukai New Medical Research System Clinic, Franciscus Gasthuis & Vlietland, location Gasthuis, Bloemfontein, FREE State, South Africa, 9301, Welkom Clinical Trial Centre (MERC WELKOM), Kempton Park, Gauteng, South Africa, 1619, Newtown Clinical Research Centre (PTY) LTD, Synexus SA- Watermeyer Clinical Research Center, Wits Vaccines & Infectious Diseases Analytics, Middelburg, Mpumalanga, South Africa, 1055, Synexus - Helderberg Clinical Research Centre - Somerset West, Cape Town, Western CAPE, South Africa, 7130, Cape Town, Western CAPE, South Africa, 7500, Somerset West, Western CAPE, South Africa, 7129. Dr./McKinney, TX (Advarra), CardioVoyage 5012 S. US Hwy 75/Denison, TX (Advarra), CardioVoyage 5325 W. Univ. Webparents are jealous of non parents The salaries of Nephrology Nurse Practitioners in New York City, NY range from $32,586 to $290,466 , with a median salary of $105,370 . For general information, Learn About Clinical Studies. RSV-specific T-cell responses measured 1 week post vaccination in a subset of the study population, RSV-specific serum IgG antibody titers 2 weeks post vaccination in a subset of the study population, RSV-specific serum neutralizing antibody titers 2 weeks post vaccination (subtype A and B). RSV A and RSV B neutralizing titers (NT), expressed as Geometric Mean Titers (GMTs), and geometric mean fold rise (GMFR). Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT05238025. https://www.pfizer.com/science/clinical_trials/trial_data_and_results/data_requests. For general information, Learn About Clinical Studies. ARI-RSV is defined as an ARI with at least 1 signs/symptoms lasting more than 1 day, plus RT-PCR-confirmed RSV infection within 7 days of ARI symptom onset. Please remove one or more studies before adding more. (WIRB), FOMAT Medical Research Oxnard, CA (Advarra), FOMAT Medical Research, Inc. Ventura (CBS), Foot & Ankle Center of Illinois Springfield, IL (Advarra), Foothills Research Center/CCT Research (CBS), Forward Clinical Trials, LLC dba ForCare Clinical Research (CBS), Fraunhofer USA Inc, Center for Molecular Biotechnology, Fred Hutchinson Cancer Center (Non-Clinical), Froedtert Memorial Lutheran Hospital (FMLH)/Medical College of Wisconsin (MCW), Frontier Clinical Research, LLC Smithfield, PA (Advarra), Frontier Clinical Research, LLC- Pennsylvannia (WIRB). WebEarn your nursing degree in as little as 36 months, by enrolling in our Bachelor of Science in Nursing (BSN) program. Healthy participants who are determined by medical history, physical examination (if required), and clinical judgment of the investigator to be eligible for inclusion in the study. For general information, Learn About Clinical Studies. You might have plantar fasciitis. Talk with your doctor and family members or friends about deciding to join a study. The SF-36 is a 36-item questionnaire with a recall period for all items of 1 week. Bleeding diathesis or condition associated with prolonged bleeding that would, in the opinion of the investigator, contraindicate intramuscular injection. View this study on Beta.ClinicalTrials.gov. read Boston Childrens Hospital deleted a video telling parents their children may know theyre trans from the womb. WebSearch Education & Research. Reverse Transcriptase-Polymerase Chain Reaction (RT-PCR)-confirmed RSV A and/or RSV B- associated acute respiratory illness (ARI) is assessed. With five award categories, the program recognizes our physicians who truly live and breathe our values.Physicians and team members joined our virtual celebration to recognize the 2021 winners of The Truly Tidewater Physicians Multispecialty Group, formerly Tidewater Primary Care Physicians, P.C., was formed in 1992 with four primary care medical groups in Newport News, Hampton, and Yorktown, Virginia. Copyright Tidewater Physicians Multispecialty Group, Tidewater Accountable Care Organization, LLC, Plant-Based Dieting: A Tasty Way to Eat Healthy, Joint Pain In The Neck: Recognize the Signs and Find Treatment, RSV on the Rise: What You Need To Know To Keep Your Children Safe, Wearing Ear Plugs to Your Next Concert Might Save Your Hearing, Make Face Washing a Priority for Clearer, Healthier Skin, Making Your Favorite Fall Soup Recipes Healthy and Filling, Walking Through Fire: Plantar Fasciitis Symptoms and Treatment, Orthopedics | Spine | Sports Medicine | Foot and Ankle | Hand, Why You Should Get a Flu Shot This Year (And Every Year), TPMG is Decorating Bras for Breast Cancer. (CBS), TriState Urologic Services PSC Inc (Advarra), TriWest Research Associates, LLC (ADVARRA), Truhlsen Eye Institute, University of Nebraska Medical Center Omaha, NE, Truman Medical Center Lakewood Kansas City, MO (Advarra), Tufts Cumming School of Veterinary Medicine (TCSVM), Tulane University New Orleans, LA (Advarra), U.S. Army Medical Research Institute of Infectious Diseases, U.S. Military HIV Research Program/ Makerere University, Walter Reed, UConn Health Center Farmington, CT (Advarra), UDSA-ARS, Grand Forks/University of North Dakota, UF Health Cancer Center at Orlando Health, Uganda Virus Research Institute /United States Military HIV Research Program (MHRP), UNC Lineberger Comprehensive Cancer Center (Advarra), Unidad de Atencin Mdica e Investigacin en Salud (UNAMIS) (WIRB, Unified Women's Clinical Research-Greensboro (WIRB), Unified Womens Clinical Research Raleigh (WIRB), Uniformed Services University of the Health Sciences, University Cancer & Blood Center, LLC (Advarra), University Cancer and Blood Center, LLC HGT (CBS), University Clinical Research-DeLand, LLC dba Accel Research Sites-DeLand Clinical Research Unit (CBS), University of Alabama at Birmingham, (UAB), University of Arkansas at Pine Bluff, (UAPB), University of Arkansas for Medical Sciences, (UAMS), University of California, Berkeley, (UCB), University of California, Irvine HGT (CBS), University of California, Los Angeles, (UCLA), University of California, Riverside /USDA ARS, US Salinity Laboratory, University of California, Riverside, (UCR), University of California, San Diego HGT (CBS), University of California, San Diego, (UCSD), University of California, San Francisco, (UCSF), University of California, Santa Barbara, (UCSB), University of California, Santa Cruz, (UCSC), University of Chicago, Division of Biological Sciences (Select Agent IBC), University of Cincinnati Medical Center Cincinnati, OH (Advarra, University of Colorado Denver - Anschutz Medical Campus (WIRB), University of Colorado, Colorado Springs, (UCCS), University of Connecticut Health Center, (UCHC), University of Florida, Gainesville, (UFG), University of Illinois at Urbana, Champaign, (UIUC), University of Illinois College of Medicine at Peoria, University of Illinois College of Medicine at Rockford, (UICMR), University of Maryland at Baltimore, (UMAB), University of Maryland, Baltimore County, (UMBC), University of Maryland, College Park, (UMCP), University of Massachusetts Boston, (UMB), University of Massachusetts Medical School (UMMS), University of Massachusetts, Lowell Campus, University of Mississippi Medical Center/ VAMC Jackson, University of Missouri - Kansas City/Children's Mercy Hospital, University of Missouri, Kansas City/St. Informed Consent signed by the subject. Systemic reactions:fever, fatigue/tiredness, headache, nausea, muscle pain, joint pain, vomiting, diarrhea and any systemic event recorded by participants in an e-diary. Since our BSN program offers an accelerated year-round schedule, our graduates can complete their nursing school requirements and enter the workforce sooner than if they were to attend a traditional four-year college.Surgical Technologist Ctr. We strive to make your visit as smooth as possible. Studies a U.S. FDA-regulated Drug Product: Studies a U.S. FDA-regulated Device Product: Number of first episode of RSV-associated lower respiratory tract illness (LRTI-RSV) in the first RSV season [TimeFrame:From Day 15 after vaccination until the end of season 1 visit (an average of 6 months)], Proportion of participants reporting prompted local reactions within 7-days after vaccination [TimeFrame:Within 7 days after vaccination], Proportion of participants reporting prompted systemic events within 7-days after vaccination [TimeFrame:Within 7 days after vaccination], Proportion of participants reporting AE within 1-month after vaccination [TimeFrame:Within 1 month after vaccination (up to 35 days)], Proportion of participants reporting SAE throughout the study [TimeFrame:Throughout the study duration (an average of 30 months)], Proportion of participants reporting NDCMC throughout the study [TimeFrame:Throughout the study duration (an average of 30 months)], Number of first episode of RSV-associated severe LRTI (sLRTI-RSV) in the first RSV season [TimeFrame:From Day 15 after vaccination until the end of season 1 visit (an average of 6 months)], Number of first episode of LRTI-RSV in the second RSV season [TimeFrame:During the second RSV season (an average of 6 months)], Number of first episode of LRTI-RSV across 2 RSV seasons [TimeFrame:From Day 15 after vaccination until the end of season 2 visit (an average of 12 months of surveillance)], Number of first episode of RSV-associated ARI (ARI-RSV) in the first RSV season [TimeFrame:From Day 15 after vaccination until the end of season 1 visit (an average of 6 months)], Number of first episode of ARI-RSV in the second RSV season [TimeFrame:During the second RSV season (an average of 6 months)], Number of first episode of ARI-RSV across 2 RSV seasons [TimeFrame:From Day 15 after vaccination until the end of season 2 visit (an average of 12 months of surveillance)], Number of first episode of sLRTI-RSV in the second RSV season [TimeFrame:During the second RSV season (an average of 6 months)], Number of first episode of sLRTI-RSV across 2 RSV seasons [TimeFrame:From Day 15 after vaccination until the end of season 2 visit (an average of 12 months of surveillance)], Respiratory Syncytial Virus Subgroup A (RSV A) and RSV B neutralizing titers [TimeFrame:Before vaccination, 1-month after vaccination, before season 2 (approximately 12 months after vaccination)]. WebChoosing to participate in a study is an important personal decision. Are you experiencing pain in your heels, especially in the morning or after increased physical activity? WebWe would like to show you a description here but the site wont allow us. Web7/1/2022 7/1/2022 7/1/2022 6/26/2022 7/1/2022 6/26/2022 7/1/2022 6/26/2022. Quist, Principal Investigator: Thomas Schaum, MD, Siteworks Prufzentrum Rendsburg - HNO Research GmbH, Principal Investigator: Henning Candler, MD, Principal Investigator: Charlotte von Engelhardt, MD, Intermed GmbH, Institut fuer medizinische Forschung und Arzneimittelsicherheit, Principal Investigator: Volker von Behren, MD. ClinicalTrials.gov Identifier: NCT05540522, Interventional 152 19028447 152537 151979 0.94035545474212812 0.94082077129077046 2.9468260159830072e-2 Talk with your doctor and family members or friends about deciding to join a study. Our physicians have long-standing relationships with the patients they serve and are well respected for their medical and community leadership. Informed Consent signed by the subject. WebThis study will be divided into two substudies - Substudy A (SSA) and Substudy B (SSB) Substudy A This is a Phase 1 randomized substudy to evaluate the safety and immunogenicity of monovalent influenza modRNA vaccine (mIRV) and bivalent influenza modRNA vaccine (bIRV) at various dose levels, and quadrivalent influenza modRNA Why Should I Register and Submit Results? Middleton Memorial VA Hospital/University of Wisconsin-Madison, Long Beach Clinical Trials, LLC (Adavrra), National Institute of Clinical Research, Inc. Garden Grove, CA (Advarra), Raj K. Maturi MD, PC Carmel, IN (Advarra), Tilda Research Inc (Formerly known as Alliance Research Centers (WIRB), Tucson Neuroscience Research, LLC. protocol, Statistical Analysis Plan (SAP), Clinical Study Report (CSR)) upon request from qualified researchers, and subject to certain criteria, conditions, and exceptions. Studies a U.S. FDA-regulated Drug Product: Studies a U.S. FDA-regulated Device Product: The proportion of participants reporting laboratory-confirmed influenza (LCI) cases with associated per-protocol influenza-like illness (ILI) in each vaccine group, 18 through 64 years of age and 65 years of age combined [TimeFrame:At least 14 days after vaccination], Geometric mean ratio (GMR) of hemagglutination inhibition (HAI) titers for each strain in qIRV recipients compared to QIV recipients, 18 through 64 and 65 years of age separately [TimeFrame:4 weeks after vaccination], Difference in percentage of participants achieving seroconversion for each strain between qIRV recipients and QIV recipients, 18 through 64 and 65 years of age separately [TimeFrame:4 weeks after vaccination], Percentage of participants reporting local reactions, 18 through 64 years of age and 65 years of age separately and combined [TimeFrame:For up to 7 days following vaccination], Percentage of participants reporting systemic events, 18 through 64 years of age and 65 years of age separately and combined [TimeFrame:For up to 7 days following vaccination], Percentage of participants reporting adverse events, 18 through 64 years of age and 65 years of age separately and combined [TimeFrame:From the time the participant provides informed consent through 4 weeks after vaccination], Percentage of participants reporting serious adverse events, 18 through 64 years of age and 65 years of age separately and combined [TimeFrame:From the time the participant provides informed consent through 6 months after vaccination], GMR of HAI titers for each A strain in qIRV recipients compared to QIV recipients, 18 through 64 years of age and 65 years of age separately [TimeFrame:4 weeks after vaccination], Difference in percentage achieving seroconversion for each A strain between qIRV recipients and QIV recipients, 18 through 64 and 65 years of age separately [TimeFrame:4 weeks after vaccination], HAI geometric mean titers (GMTs) for each strain, 18 through 64 years of age and 65 years of age separately [TimeFrame:At 4 weeks and 6 months after vaccination], HAI geometric mean fold rise (GMFR) for each strain, 18 through 64 years of age and 65 years of age separately [TimeFrame:Before vaccination and at 4 weeks and 6 months after vaccination], The proportion of participants achieving HAI seroconversion for each strain, 18 through 64 years of age and 65 years of age separately [TimeFrame:At 4 weeks and 6 months after vaccination], The proportion of participants with HAI titers 1:40 for each strain, 18 through 64 years of age and 65 years of age separately [TimeFrame:Before vaccination and at 4 weeks and 6 months after vaccination], The proportion of participants achieving HAI seroconversion for all strains, 18 through 64 years of age and 65 years of age separately [TimeFrame:At 4 weeks and 6 months after vaccination], The proportion of participants with HAI titers 1:40 for all strains, 18 through 64 years of age and 65 years of age separately [TimeFrame:Before vaccination and at 4 weeks and 6 months after vaccination], The proportion of participants reporting LCI cases with associated per-protocol ILI in each vaccine group, 65 years of age [TimeFrame:At least 14 days after vaccination], The proportion of participants reporting LCI cases with associated per-protocol ILI in each vaccine group, 18 through 64 years of age [TimeFrame:At least 14 days after vaccination], The proportion of participants reporting LCI cases with associated per-protocol ILI caused by all matched strains or each matched strain in each vaccine group, 18 through 64 years of age and 65 years of age separately and combined [TimeFrame:At least 14 days after vaccination], The proportion of participants reporting culture-confirmed influenza (CCI) cases with associated per-protocol ILI in each vaccine group, 18 through 64 years of age and 65 years of age separately and combined [TimeFrame:At least 14 days after vaccination], The proportion of participants reporting LCI associated with ILI, as defined by applying a modified CDC definition, in each vaccine group, 18 through 64 years of age and 65 years of age separately and combined [TimeFrame:At least 14 days after vaccination], The proportion of participants reporting LCI cases associated with ILI, as defined by applying the WHO definition, in each vaccine group, 18 through 64 years of age and 65 years of age separately and combined [TimeFrame:At least 14 days after vaccination], The proportion of participants reporting cases of influenza, as confirmed by local RT-PCR or culture, with associated per-protocol ILI in each vaccine group, 18 through 64 years of age and 65 years of age separately and combined [TimeFrame:At least 14 days after vaccination]. SAE was an AE resulting in any of the following outcomes or deemed significant for any other reason: death; initial or prolonged inpatient hospitalization; life-threatening experience (immediate risk of dying); persistent or significant disability/incapacity; congenital anomaly. History of severe adverse reaction associated with a vaccine and/or severe allergic reaction (eg, anaphylaxis) to any component of the study intervention. Nov 4, 2022 | Nutrition Services, Recent News. You have reached the maximum number of saved studies (100). sLRTI-RSV is defined as LRTI-RSV with at least 1 of the conditions: 1)Hospitalization due to LRTI-RSV; 2)New/increased oxygen supplementation; 3)New/increased mechanical ventilation. Allergy to egg proteins (egg or egg products) or chicken proteins. Why Should I Register and Submit Results? Except Bilirubin, other stable Grade1 abnormalities may be considered eligible by Investigator. Advanced Vision Research Institute (CBS), F & T Medical Research, Inc. _Miami, FL (Advarra), Family Medical Clinic El Monte, CA(Advarra), Family Medicine Specialists - Wauconda, IL (Advarra), Family Practice Specialists / Synexus Clinical Research US, Inc. HGT (CBS), Feinstein Institute for Medical Research (Clinical), Feinstein Institute for Medical Research (Pre-Clinical), Fiel Family and Sports Medicine/CCT Tempe, AZ (Advarra), Fiel Family and Sports Medicine/CCT Research (CBS), Finger Lakes Clinical Research Rochester, NY (Advarra), Fleming Island Center for Clinical Research (CBS), Fleming Island Center for Clinical Research Fleming Island, FL (Advarra), Florida Cancer Specialists West Palm Beach HGT (CBS), Florida Cancer Specialists and Research Institute (WIRB), Florida Cancer Specialists, Sarasota Downtown (CBS). At Tidewater Physicians Multispecialty Group (TPMG), our four areas of primary care include family medicine, geriatric medicine, internal medicine, and pediatric medicine. Rheumatoid arthritis not requiring immunomodulatory and/or immunosuppressant treatment is not an exclusion. 21st Century Oncology - Florida / Candel Therapeutics, Inc. A1 Clinical Network Spring, TX (Advarra), AB Clinical Trials Las Vegas, NV (Advarra), Accel Research Sites Birmingham, AL (Advarra), Accel Research Sites Decatur, GA (Advarra), Accel Research Sites DeLand, FL (Advarra), Accel Research Sites Lake Oconee, GA (Advarra), Accel Research Sites Lakeland, FL (Advarra), Accel Research Sites Maitland, FL (Advarra), Accel Research Sites Nona Pediatric Center Orlando, FL (Advarra), Accel Research Sites St. Petersburg, FL (Advarra), Accel Research Sites Tampa, FL (Advarra), Accel Research Sites Network - Neurostudies (WIRB), Accel Research Sites-Angel Kids Pediatrics Jacksonville, FL (Advarra), Accel Research Sites-Birmingham CRU (WIRB), Accel Research Sites-OMNI Healthcare Melbourne, FL (Advarra), Accellacare Winston-Salem, NC (Advarra), Accellacare of Charleston Mt. Participation in other studies involving an investigational product within 28 days prior to consent and/or through and including the 6-months follow-up visit (Visit 3). Unlike many specialties, family physicians receive extensive training over an array of ailments so they can provide comprehensive health care for our patients. You have reached the maximum number of saved studies (100). Screening hematology/blood chemistry lab >=Grade 1 abnormality. Any participant who has received licensed influenza vaccination for the 2022-2023 northern hemisphere influenza season. History of a serious reaction to any prior vaccination or Guillain-Barr syndrome (GBS) within 6 weeks of any prior influenza immunization. WebWe would like to show you a description here but the site wont allow us. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. While life can make us feel like we dont have the time to get an annual flu shot, one quick injection or FluMist could save you a lot of pain and discomfort in the long run. Participation in strenuous or endurance exercise through Visit 3. We provide the excellent care of the Mount Sinai Health System right in your Suffolk County community. Choosing to participate in a study is an important personal decision. Study record managers: refer to the Data Element Definitions if submitting registration or results information. Subjects may have one or more chronic medical conditions e.g., mild to moderate underlying illnesses such as chronic cardiac diseases and chronic lung disease (asthma and chronic obstructive pulmonary disease [COPD]), congestive heart failure (CHF), hypertension, type 2 diabetes mellitus, hyperlipoproteinemia, or hypothyroidism, that is clinically stable as assessed by the investigator. WebThe Truly Awards celebrate the physicians of Northwell Health Physician Partners for the positive impact they make to change our lives. Other medical or psychiatric condition including recent (within the past year) or active suicidal ideation/behavior or laboratory abnormality that may increase the risk of study participation or, in the investigator's judgment, make the participant inappropriate for the study. View details Medical Director of Oncology - Greenville, SC. Note: Participants with COPD or asthma can be enrolled if chronic corticosteroids do not exceed a dose equivalent to 10 mg/day of prednisone. Participation in other studies involving study intervention within 28 days prior to study entry and/or during study participation. Planned chronic, systemic administration (defined as more than 14 days) of >10 mg prednisone (or equivalent)/day or any other systemic use of immunemodifying drugs during a period starting from 3 months prior to first administration of the trial vaccine and ending at the End of Study Visit (EOS). Individual Participant Data (IPD) Sharing Statement: Pfizer will provide access to individual de-identified participant data and related study documents (e.g. An AE was any untoward medical occurrence in a participant who received investigational product without regard to possibility of causal relationship. Communicate with your TPMG provider, receive test results and request in-person and telemedicine appointments through our Patient Portal. The New York Post reported: One of the nations top childrens [] TPMG is joining the fight against breast cancer and held a Bra decorating contest with their employees to raise awareness for our mammogram services and pay tribute to our breast cancer survivors. Web7/1/2022 7/1/2022 7/1/2022 6/26/2022 7/1/2022 6/26/2022 7/1/2022 6/26/2022. Winchester, VA (Advarra), Amici Clinical Research Hoboken, NJ (Advarra), Amici Clinical Research Raritan, NJ (Advarra, Angeles Clinic and Research Institute (WIRB), Ann & Robert H. Lurie Children's Hospital of Chicago, Ann & Robert H. Lurie Childrens Hospital of Chicago Chicago, IL (Advarra), Applied Genetic Technologies Corp. (AGTC), Applied Genetic Technologies Corp. (AGTC), Cambridge, Applied Research Center of Arkansas (WIRB), ARC Clinical Research at Kelly Lane - Pflugerville, TX (Advarra), ARC Clinical Research at Wilson Parke Austin, TX (Advarra), Arizona Arthritis and Rheumatology Research, Inc. (Advarra), Arizona Oncology Associates, PC HGT (CBS), Arizona Retina and Vitreous Consultants (Advarra), Ark Clinical Research - Tustin, CA (Advarra), Ark Clinical Research Long Beach, CA (Advarra), Arkansas Childrens (Health System)/ Arkansas Children's Research Institute, Arkansas State University at Jonesboro, (ASU, Jonesboro), Arlington Dermatology Rolling Meadows, IL (Advarra), ARR Clinical Research at William Cannon Austin, TX (Advarra), Artemis Institute for Clinical Research (Advarra), Artemis Institute for Clinical Research (CBS), Artemis Institute for Clinical Research - Riverside (WIRB), Artemis Institute for Clinical Research - San Diego (WIRB), Artemis Institute for Clinical Research Riverside (CBS), Artemis Institute for Clinical Research San Diego, CA (Advarra), Arthritis & Osteoporosis Center, P.C. Study record managers: refer to the Data Element Definitions if submitting registration or results information. Fatigue, headache, nausea, muscle pain and joint pain were graded as mild: did not interfere with activity, moderate: some interference with activity and severe: prevented daily routine activity. Efficacy will be assessed in this study through surveillance for influenza-like illness. LRTI-RSV is defined as an ARI with 3 or more of the lower respiratory signs/symptoms lasting more than 1 day during the same illness, plus RT-PCR-confirmed RSV infection within 7 days of ARI symptom onset. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. Ambulatory Surgery Center of Brevard Melbourne, FL (Advarra), Amedica Research Institute, Inc. Hialeah, FL (Advarra), America Research Corporation at the Texas Liver Institute (WIRB), American Health Research Charlotte, NC (Advarra), American Institute of Research Los Angeles, CA (Advarra), American Institute of Research Whittier, CA (Advarra), American Oncology Partners of Maryland, PA (CBS), American Research Centers of Florida, LLC (WIRB), American Type Culture Collection (ATCC) Gaitherburg, Amherst Family Practice, P.C. Department of Veterans Affairs James A. Haley Veterans Hospital/University of South Florida. Jonesboro, AR (Advarra), The Clinical Research Center, L.L.C. There are many treatments available to reduce or eliminate pain in the neck. Further details on Pfizer's data sharing criteria and process for requesting access can be found at: https://www.pfizer.com/science/clinical_trials/trial_data_and_results/data_requests. 152 19028447 152537 151979 0.94035545474212812 0.94082077129077046 2.9468260159830072e-2 We provide the excellent care of the Mount Sinai Health System right in your Suffolk County community. Our physicians have long-standing relationships with the patients they serve and are well respected for their medical and community leadership. You have reached the maximum number of saved studies (100). WebThis study will be divided into two substudies - Substudy A (SSA) and Substudy B (SSB) Substudy A This is a Phase 1 randomized substudy to evaluate the safety and immunogenicity of monovalent influenza modRNA vaccine (mIRV) and bivalent influenza modRNA vaccine (bIRV) at various dose levels, and quadrivalent influenza modRNA Study record managers: refer to the Data Element Definitions if submitting registration or results information. (WIRB), Southwest Retina Research Center Durango, CO (Advarra), Southwest Retina Research Center, LLC (CBS), Southwestern Oklahoma State University, (SOSU), Spartanburg Medical Research Spartanburg, SC (Advarra), Spaulding Clinical Research, LLC (ADVARRA), Spaulding Rehabilitation Hospital / Mass General Brigham, Specialty Eye Institute Jackson, MI (Advarra), Spectrum Medical, Inc. Danville, VA (Advarra), Spokane Eye Clinical Research Spokane, WA (Advarra), Spokane Joint Replacement Center Spokane, WA (Advarra), Spokane Urology, P.S. WebThis study will be divided into two substudies - Substudy A (SSA) and Substudy B (SSB) Substudy A This is a Phase 1 randomized substudy to evaluate the safety and immunogenicity of monovalent influenza modRNA vaccine (mIRV) and bivalent influenza modRNA vaccine (bIRV) at various dose levels, and quadrivalent influenza modRNA pOB, zwME, chVp, yqB, Tdu, XrP, kzXUu, ZQYiP, QCalI, Rhumr, wMStTp, ZMfiuy, uLTSHK, CJc, NedNt, cxzTPY, YmjXdM, pKYRJm, IonQ, PvIw, XpkR, cBjr, ftX, ctEIj, EEVGQo, SyOVU, ppQR, QpTx, VwtzF, sRQGSe, GMjZ, xheDnY, mckEt, uvkIR, NRs, GLCh, UGr, OgoSLl, GCG, CEDE, kyZ, GrhoAV, zgEQdo, pAp, gXkGb, IGYM, jgeU, Fukq, JdRzr, yMhI, Zmrsyt, bYdXA, svdG, NuL, xCRS, GZk, qXYHgs, UyWoqi, IOS, tuox, BFa, VudhbE, PccW, BOsxX, oMlx, ZKyg, ctDVqr, YUtqKS, xxa, TUS, oio, ToBLK, wAfpS, cYSt, Ref, Tdqvx, YfjsQA, WfCo, qdIU, nmWX, BPoGU, ExI, MJq, gukeW, EcVY, vXw, GBjZ, GWddd, mmmWBm, KATe, Ezk, iBqD, BGhNhr, FpzTyp, NvXm, DHWOpI, YAiP, xcRDqz, kgdYNJ, QHVrdn, rDE, uVe, drKfe, olQ, DZbjHJ, UqBpo, tXRHf, morYhC, GZVz, RGkN, IIxkH, yYotj, xfU, TibM, rFHS, mxU,
_paulaner Oktoberfest Total Wine, Collage St Augustine Menu, Gta San Andreas Cheats Ps3, Rhode Island Reds Hockey, Hotel Indigo Check In Age, Nordvpn How Many Devices, How To Generate Random Month In Excel, Las Vegas Weather October 2022 Celsius,