Clinical Trials Directory

Trials / Completed

CompletedNCT01218906

Prospective Surveillance of Febrile Illness for Dengue-Endemic Areas in Asia

Status
Completed
Phase
Study type
Observational
Enrollment
1,500 (actual)
Sponsor
Sanofi · Industry
Sex
All
Age
2 Years – 14 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to detect acute febrile episodes and dengue infection in five Asian countries, to assess dengue seroprevalence, and to assess surveillance infrastructure at investigational sites in anticipation of a Phase 3 efficacy trial of a vaccine to prevent dengue infection. The primary objectives are: * To identify acute febrile episodes among the cohort in order to detect the presence of dengue infection. * To develop operational infrastructure for potential Phase III dengue efficacy trial sites. * To describe the dengue seroprevalence among the cohort at baseline and at the end of the study.

Detailed description

All participants will make two visits to a study site, an enrollment visit and a termination visit. Additional visits will be made if febrile episodes occur: an acute visit and a convalescent visit. Participants or their parents/guardians will be contacted weekly to monitor the occurrence of febrile episodes and ensure appropriate assessment and care. No vaccine will be provided or administered in this study.

Conditions

Timeline

Start date
2010-08-01
Primary completion
2011-11-01
Completion
2012-03-01
First posted
2010-10-11
Last updated
2018-01-16

Locations

11 sites across 5 countries: Indonesia, Malaysia, Philippines, Thailand, Vietnam

Source: ClinicalTrials.gov record NCT01218906. Inclusion in this directory is not an endorsement.