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Study to Determine The Effectiveness Of Detrusitol In Patients Diagnosed With OAB

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Viatris

Status and phase

Completed
Phase 4

Conditions

Urinary Incontinence

Treatments

Drug: tolterodine SR, overactive bladder

Study type

Interventional

Funder types

Industry

Identifiers

NCT00143377
A6121122

Details and patient eligibility

About

The purpose of this study is to evaluate the effectiveness of Detrusitol (tolterodine tartrate) SR, 4 mg once daily, on patient's perception of the symptoms of overactive bladder and which of these bothersome symptoms are improved with treatment.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 years or older patients suffering from OAB symptoms (urinary frequency of at least 8 micturitions per 24h, urinary urgency and at least 3 urge urinary incontinence episodes within 3 days), confirmed by a micturition bladder diary.

Exclusion criteria

  • Other than urge incontinence
  • History of prostate/uterine or other female organ cancer

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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