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RecruitingNCT06928753

Real-world Effectiveness, Safety and Immunogenicity of Chikungunya Vaccination in Populations at Risk of Severe or Complicated Forms: Prospective Study in La Réunion

Status
Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
1,800 (estimated)
Sponsor
Centre Hospitalier Universitaire de la Réunion · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Against the backdrop of a growing chikungunya epidemic in La Réunion, this prospective study will assess the real-life efficacy, safety and immunogenicity of IXCHIQ® vaccine in vulnerable individuals (seniors, comorbid patients), defined by the French Health Autority (HAS) as at risk of severe or complicated forms and/or chronic disabling forms (chronic arthritis, chronic fatigue phenotypes). This study will also provide input for the preparation of a cluster randomized trial on a population scale.

Conditions

Interventions

TypeNameDescription
BIOLOGICALIXCHIQGroup of vaccinated arm will be with the IXCHIQ vaccine

Timeline

Start date
2025-04-18
Primary completion
2026-04-01
Completion
2026-10-01
First posted
2025-04-15
Last updated
2025-07-29

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT06928753. Inclusion in this directory is not an endorsement.

Real-world Effectiveness, Safety and Immunogenicity of Chikungunya Vaccination in Populations at Risk of Severe or Compl (NCT06928753) · Clinical Trials Directory