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NOT YET RECRUITING
NCT07279298

Effectiveness of Immunization in Preventing Severe Acute Respiratory Infection RSV

Sponsor: Bogotá District Health Secretariat

View on ClinicalTrials.gov

Summary

This study aims to evaluate the real-world effectiveness of two preventive immunization strategies against Respiratory Syncytial Virus (RSV)-associated severe acute respiratory infection in infants less than six months of age in Bogotá, Colombia. The strategies include maternal vaccination with RSVpreF administered between 28 and 36 weeks of gestation and neonatal immunization with nirsevimab for infants born to mothers who did not receive RSVpreF during pregnancy. Using a test-negative case-control design embedded in the city's sentinel surveillance system, infants hospitalized for severe respiratory infection will be systematically tested for RSV. Comparative vaccine effectiveness will be estimated to determine the impact of maternal RSV vaccination and neonatal monoclonal antibody immunization on RSV-associated hospitalizations, intensive care admissions, and mortality. The study will generate real-world evidence to inform local and regional public health decisions and guide the implementation of cost-effective hybrid immunization strategies against RSV in middle-income settings.

Official title: Effectiveness of Immunization in Preventing Severe Acute Respiratory Infection Associated With Respiratory Syncytial Virus-RSV- in Infants Under 6 Months of Age in Bogotá: a Case-control Study With a Negative Test Design

Key Details

Gender

All

Age Range

1 Day - 180 Days

Study Type

OBSERVATIONAL

Enrollment

1097

Start Date

2026-02-01

Completion Date

2027-07-31

Last Updated

2025-12-12

Healthy Volunteers

No

Interventions

BIOLOGICAL

RSVpreF vaccine (Abrysvo) and Nirsevimab (Beyfortus) or unexposed

Maternal vaccination administered between 28 and 36 weeks of gestation and Single-dose monoclonal antibody administered to newborns whose mothers did not receive effective RSVpreF vaccination or unexposed