Clinical Trials Directory

Trials / Completed

CompletedNCT00524732

Assessment of the Reactogenicity of ADACEL® (TdcP Vaccine) in Children and Adolescents 7 to 19 Years of Age

Status
Completed
Phase
Study type
Observational
Enrollment
7,156 (actual)
Sponsor
Sanofi Pasteur, a Sanofi Company · Industry
Sex
All
Age
7 Years – 19 Years
Healthy volunteers
Accepted

Summary

To compare the reactogenicity of ADACEL® vaccine given at intervals of 2 to 9 years with the reactogenicity of ADACEL® vaccine given at an interval of 10 or more years following the last previous administration of vaccine containing Diphtheria and Tetanus Toxoids (referred to as TD/Td).

Conditions

Interventions

TypeNameDescription
BIOLOGICALTetanus and diphtheria toxoids and acellular pertussis0.5 mL, Intramuscular

Timeline

Start date
2004-09-01
Primary completion
2004-12-01
Completion
2005-09-01
First posted
2007-09-05
Last updated
2014-01-14

Locations

2 sites across 1 country: Canada

Source: ClinicalTrials.gov record NCT00524732. Inclusion in this directory is not an endorsement.