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NCT00282932 · ClinicalTrials.gov registry record · Phase 4

Detrol LA In Men With Overactive Bladder.

A Phase 4 study, sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris.

Completed
Registry status
Phase 4
Development phase
600
Enrollment target

NCT00282932: Completed Phase 4 study, sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris.

NCT00282932 is a Phase 4 study that has completed, run by Pfizer's Upjohn has merged with Mylan to form Viatris. The registered enrollment target is 600 participants, above the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (16% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00282932, a Phase 4 study, has completed, sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris.

COMPLETED
Registry status
Phase 4
Development phase
600 participants
Enrollment target

Study Summary

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.

Interventions

  • DRUG Detrol LA

Trial Details

FieldValue
Enrollment Target 600 participants
Start Date 2006-01
Est. Completion 2007-05-14
Phase Phase 4

What the finished NCT00282932 record still lists

NCT00282932 is an interventional study that assigns participants to a tested intervention. The registered 600 participants enrollment target is mid-sized for trials with a published cap, above the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (16% higher).

The record links to 0 conditions, and to 1 intervention - of which Detrol LA is the first listed.

NCT00282932 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00282932 about?

NCT00282932 is a clinical study titled "Detrol LA In Men With Overactive Bladder.". 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...

What is the current status of trial NCT00282932?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 600 participants. The study started on 2006-01. Estimated completion is 2007-05-14.

What interventions are being tested in trial NCT00282932?

The interventions under investigation include: Detrol LA (DRUG).

Who is sponsoring clinical trial NCT00282932?

This trial is sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris, which has 158 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00282932's enrollment target sits among peer trials

600 137th of 2000 higher than 1,854 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00282932, the US trial registry maintained by the National Library of Medicine. NCT00282932 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.