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Post Marketing Surveillance Of Fesoterodine In Filipino Patients With Over Active Bladder

Pfizer logo

Pfizer

Status

Completed

Conditions

Over Active Bladder

Treatments

Drug: Fesoterodine

Study type

Observational

Funder types

Industry

Identifiers

NCT01260311
A0221085

Details and patient eligibility

About

This is an observational study and will determine the safety profile of fesoterodine in Filipino patients prescribed the drug. This is in compliance with the requirements of the Philippine Food and Drug Administration.

Full description

Sampling method is not applicable in this study. Only patients prescribed Fesoterodine will be enrolled.

Enrollment

508 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Over-active bladder
  • Prescribed with Fesoterodine

Exclusion criteria

  • Hypersensitivity
  • Urinary retention

Trial design

508 participants in 1 patient group

Patients prescribed with Fesoterodine
Description:
Patients diagnosed with Over-active bladder and prescribed with fesoterodine.
Treatment:
Drug: Fesoterodine

Trial contacts and locations

37

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Data sourced from clinicaltrials.gov

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