Clinical trial

Real-World Effectiveness of Perinatal RSV Immunoprophylaxis

Name
2000036550
Description
The purpose of this study is to continue evaluating how well the RSV vaccines work as they are currently being used in routine clinical practice. Some of the questions that the investigators hope to answer with this study are: 1) What is the overall effectiveness of these vaccines? 2) How long does immunity last? 3) How effective are the vaccines against new strains? 3) Does the vaccine's effectiveness vary by age?
Trial arms
Trial start
2024-07-01
Estimated PCD
2028-12-30
Trial end
2028-12-30
Status
Not yet recruiting
Treatment
Nirsevimab
Immunoprophylaxis against RSV
Arms:
ARI Cases, ARI Controls, Healthy Controls
Other names:
RSV vaccines
Size
3750
Primary endpoint
Overall effectiveness of RSV immunoprophylaxis
Up to 5 years
Eligibility criteria
Inclusion Criteria: * ≤ 12 months of age at the time of presentation for evaluation for an acute respiratory infection (ARI). * Documentation of an ARI, which is defined as an acute onset (\<10 days) illness that includes: At least two of the following symptoms: fever (measured or subjective), chills, rigors, myalgia, headache, sore throat, nausea or vomiting, diarrhea, fatigue, congestion OR any one of the following: cough, shortness of breath, difficulty breathing, olfactory disorder, taste disorder, confusion, persistent chest pain, pale, gray, hypoxia, clinical or radiographic evidence of pneumonia or respiratory distress syndrome. * Residents of Connecticut Exclusion Criteria: * Illness duration of \>10 days at the time of respiratory specimen collection, measured from the date of the first symptom of the current acute illness. * Parents/guardians are not able to provide informed consent To be eligible for inclusion in the study as a healthy control, an individual must meet all of the following criteria: * Immunized against RSV ≤ 12 months of age * Residents of Connecticut * Match an enrolled case that was a vaccine failure by date of birth (±1 month), sex, and immunoprophylactic agent received (i.e., maternal vaccine vs mAb).
Protocol
{'studyType': 'OBSERVATIONAL', 'patientRegistry': False, 'designInfo': {'observationalModel': 'CASE_CONTROL', 'timePerspective': 'RETROSPECTIVE'}, 'bioSpec': {'retention': 'SAMPLES_WITH_DNA', 'description': '3,750 participants will be enrolled in this study. They will provide respiratory samples for the identification of viruses. One hundred patients will provide acute and convalescent blood.'}, 'enrollmentInfo': {'count': 3750, 'type': 'ESTIMATED'}}
Updated at
2024-04-24

1 organization

1 product

1 indication

Organization
Yale University
Product
Nirsevimab