Detrol LA In Men With Overactive Bladder.

Completed · Phase 4

Conditions studied: Overactive Bladder (OAB)

In brief

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.

Key facts

Study ID
NCT00282932
Run by
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
People needed
600
Starts
2006-01-01
Expected to finish
2007-05-14
Last updated by the study team
2021-01-27

Who can join

Age: 40 and older. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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