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NCT00224146 · ClinicalTrials.gov registry record · Phase 4

Transdermal (TDS) Oxybutynin (Oxytrol(r)) in Overactive Bladder

A Phase 4 study, sponsored by Watson Pharmaceuticals.

Completed
Registry status
Phase 4
Development phase
2,878
Enrollment target

NCT00224146: Completed Phase 4 study, sponsored by Watson Pharmaceuticals.

NCT00224146 is a Phase 4 study that has completed, run by Watson Pharmaceuticals. The registered enrollment target is 2,878 participants, above the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (456% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00224146, a Phase 4 study, has completed, sponsored by Watson Pharmaceuticals.

COMPLETED
Registry status
Phase 4
Development phase
2,878 participants
Enrollment target

Study Summary

This study evaluates changes in health related quality of life outcomes in patients using Oxytrol(r)

Interventions

  • DRUG oxybutynin transdermal delivery system (Oxytrol(r))

Trial Details

FieldValue
Enrollment Target 2,878 participants
Start Date 2004-05
Est. Completion 2005-05
Phase Phase 4
Watson Pharmaceuticals

28 total trials

What the finished NCT00224146 record still lists

NCT00224146 is an interventional study that assigns participants to a tested intervention. Its 2,878 participants enrollment target places it among the larger protocols in the corpus, above the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (456% higher).

The record links to 0 conditions, and to 1 intervention - of which oxybutynin transdermal delivery system (Oxytrol(r)) is the first listed.

NCT00224146 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00224146 about?

NCT00224146 is a clinical study titled "Transdermal (TDS) Oxybutynin (Oxytrol(r)) in Overactive Bladder". This study evaluates changes in health related quality of life outcomes in patients using Oxytrol(r)

What is the current status of trial NCT00224146?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 2,878 participants. The study started on 2004-05. Estimated completion is 2005-05.

What interventions are being tested in trial NCT00224146?

The interventions under investigation include: oxybutynin transdermal delivery system (Oxytrol(r)) (DRUG).

Who is sponsoring clinical trial NCT00224146?

This trial is sponsored by Watson Pharmaceuticals, which has 28 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00224146's enrollment target sits among peer trials

2,878 25th of 2000 higher than 1,976 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 NCT00224146, the US trial registry maintained by the National Library of Medicine. NCT00224146 (large enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.