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Descriptive, Post-marketing, Passive Surveillance Safety Study of ADACEL™ Vaccine
Descriptive, Post-marketing, Passive Surveillance Safety Study of ADACEL™ Vaccine

NCT00258882

CompletedN/A

Sponsor: Sanofi Pasteur, a Sanofi Company

Conditions: Pertussis

Interventions: Tetanus Toxoid, acellular pertussis, diphtheria toxoid

Countries: United States

To further characterize the vaccine safety profile and to identify any signals of potentially vaccine-related adverse events (AEs) not detected during pre-licensure studies.

Eligibility overview

Sex: ALL

Healthy volunteers: Yes

Study type: OBSERVATIONAL

Eligibility criteria
Inclusion Criteria:

* Receipt of ADACEL vaccine during the study period

Exclusion Criteria:

* None
Locations (3)
  • Oakland, California, United States
  • Aurora, Colorado, United States
  • Portland, Oregon, United States