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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 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.

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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 Registry Record Tells You About NCT00282932

The ClinicalTrials.gov registry entry for NCT00282932 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 600 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pfizer's Upjohn has merged with Mylan to form Viatris, which has 158 total studies on file at ClinicalTrials.gov.

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

NCT00282932 reports 0 study locations.

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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.