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TRIBIK Drug Use Surveillance

TRIBIK Drug Use Surveillance

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT1080223795
Enrollment
600
Registered
2018-02-02
Start date
2018-03-09
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diphtheria, Pertussis, Tetanus

Interventions

investigational material(s) Generic name etc : TRIBIK(Adsorbed Diphtheria-purified Pertussis-tetanus Combined Vaccine) INN of investigational material : - Therapeutic category code : 636 Mixed biologi

Sponsors

The Research Foundation for Microbial Diseases of Osaka University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Vaccinees who meet both of the following conditions [1] and [2]: [1] Vaccinees who received TRIBIK at the age of 90 months and over. [2] Vaccinees who are able to participate in a questionnaire survey on the health status after vaccination with TRIBIK ( or vaccinees whose guardians are able to participate in the questionnaire survey).

Exclusion criteria

Exclusion criteria: -

Design outcomes

Primary

MeasureTime frame
safety safety:Rate of vaccine-related adverse event, Factors that may influence safety, Rate of serious vaccine-related adverse event

Secondary

MeasureTime frame
other -

Countries

Japan

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026