Status:

COMPLETED

Tolterodine Drug Use Investigation.(Post Marketing Commitment Plan)

Lead Sponsor:

Pfizer's Upjohn has merged with Mylan to form Viatris Inc.

Conditions:

Overactive Bladder

Eligibility:

All Genders

Brief Summary

The objective of this surveillance is to collect information about 1) adverse drug reaction not expected from the Package Insert (unknown adverse drug reaction), 2) the incidence of adverse drug react...

Detailed Description

All the subjects whom an investigator prescribes the first Detrusitol Capsule should be registered consecutively until the number of subjects reaches target number in order to extract patients enrolle...

Eligibility Criteria

Inclusion

  • Male or female subjects intend to treat their overactive bladder who are prescribed Detrusitol Capsule by their physicians.

Exclusion

  • Subjects who have been prescribed Detrusitol Capsule before.

Key Trial Info

Start Date :

December 1 2006

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

March 1 2011

Estimated Enrollment :

11157 Patients enrolled

Trial Details

Trial ID

NCT01488578

Start Date

December 1 2006

End Date

March 1 2011

Last Update

January 28 2021

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