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Completed Phase 4 Interventional Accepts healthy volunteers Results available

Study of DAPTACEL® Administered as a 5th Dose in 4 to 6-Year-Old Children Previously Immunized With PENTACEL™

ClinicalTrials.gov ID: NCT00802867

Public ClinicalTrials.gov record NCT00802867. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 2:12 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Safety and Immunogenicity of DAPTACEL® (CP10/5/5/3DT Aventis Pasteur 5-component Pertussis Vaccine in Combination With Tetanus and Diphtheria Toxoids Adsorbed) Administered as a 5th Dose in 4 to 6-Year-Old Children Previously Immunized With PENTACEL™ (HCP20/20/5/3DT-mIPV//PRP-T)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Objectives: * To present the rates of adverse reactions after a dose of DAPTACEL® vaccine administered to children 4 to 6 years of age who have previously received four doses of PENTACEL™ vaccine. * To present immunogenicity before and after a single dose of DAPTACEL® vaccine administered to children 4 to 6 years of age who have previously received four doses of PENTACEL™ vaccine.

Study identification

NCT ID
NCT00802867
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Enrollment
989 participants

Conditions and interventions

Eligibility (public fields only)

Age range
4 Years to 6 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 2004 (Type not available)
Primary completion
Jun 2005 (Actual)
Completion
Sep 2005 (Actual)
Last update posted
Apr 14, 2016

2004 – 2005

United States locations

U.S. sites
19
U.S. states
14
U.S. cities
19
Facility City State ZIP Site status
Not listed Jonesboro Arkansas 72401 —
Not listed Little Rock Arkansas 72205 —
Not listed Oakland California 94612 —
Not listed Torrance California 90502 —
Not listed Orlando Florida 32806 —
Not listed Atlanta Georgia 30322 —
Not listed Boston Massachusetts 02115 —
Not listed Woburn Massachusetts 01801 —
Not listed Omaha Nebraska 68131 —
Not listed Albany New York 12208 —
Not listed Rochester New York 14620 —
Not listed Chapel Hill North Carolina 27514 —
Not listed Sylva North Carolina 28779 —
Not listed Pittsburgh Pennsylvania 15241 —
Not listed Nashville Tennessee 37232 —
Not listed San Antonio Texas 78205 —
Not listed Layton Utah 84041 —
Not listed Vancouver Washington 98664 —
Not listed Marshfield Wisconsin 54449 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00802867, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 14, 2016 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00802867 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →