id.DRIVE RSV Vaccine Effectiveness Study
Research type
Research Study
Full title
Brand-specific respiratory syncytial virus vaccine effectiveness in Europe A contribution of id.DRIVE, a public-private partnership to facilitate the conduct of observational studies on infectious diseases, vaccines, related preventive measures and therapeutics for infectious diseases in Europe
IRAS ID
343291
Contact name
Thomas Verstraeten
Contact email
Sponsor organisation
P95
Clinicaltrials.gov Identifier
1000000035, EUPAS
Duration of Study in the UK
1 years, 0 months, 1 days
Research summary
This protocol describes a European, non-interventional study to estimate the effectiveness of vaccines) against respiratory syncytial virus (RSV). Of interest is the effectiveness against hospitalisation due to severe acute respiratory infection (SARI) caused by RSV. The study is a multi-country, hospital-based study with test-negative case-control (TNCC) design.
REC name
London - Brighton & Sussex Research Ethics Committee
REC reference
24/PR/1101
Date of REC Opinion
7 Mar 2025
REC opinion
Further Information Favourable Opinion