ClinicalTrials.Veeva

Menu

Evaluate Efficacy and Safety Of Tolterodine Extended Release Capsule Compared With Tolterodine Immediate Release Tablet

Viatris logo

Viatris

Status and phase

Completed
Phase 3

Conditions

Urinary Incontinence

Treatments

Drug: tolterodine extended release capsule

Study type

Interventional

Funder types

Industry

Identifiers

NCT00139724
A6121112

Details and patient eligibility

About

To evaluate efficacy of tolterodine extended release formulation compared with immediate release formulation in subjects with symptoms of overactive bladder

Enrollment

260 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subjects with a diagnosis of overactive bladder.

Exclusion criteria

  • Subjects with significant stress incontinence as determined by the investigator.
  • Subjects with recurrent urinary tract infections defined as treated for UTI; 5 times in the last year.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

Trial contacts and locations

7

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems