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Detrol LA In Men With Overactive Bladder.

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Viatris

Status and phase

Completed
Phase 4

Conditions

Overactive Bladder (OAB)

Treatments

Drug: Detrol LA

Study type

Interventional

Funder types

Industry

Identifiers

NCT00282932
A6121127

Details and patient eligibility

About

An interventional active/placebo double blinded parallel randomized controlled study in which at 12 weeks of treatment, the primary endpoint of patient perception of bladder condition is measured along with associated safety and other secondary endpoints like bladder diary endpoints, quality of life and patient treatment satisfaction.

Patients included in the study must have symptoms of OAB (frequency of at least 8 per day and Urgency of at least 1 episode per day confirmed by bladder diary).

Patients are not eligible to enroll in the study if they have/had significant hepatic or renal disease, history of radiation treatment.

Sex

Male

Ages

40+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Symptoms of OAB (frequency more than 8 per day and Urgency more than 1 episode per day confirmed by bladder diary)

Exclusion criteria

  • Significant hepatic or renal disease, history of radiation treatment

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

Trial contacts and locations

81

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Data sourced from clinicaltrials.gov

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