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NCT00536484 · ClinicalTrials.gov registry record · Phase 3

Fesoterodine Flexible Dose Study

A Phase 3 study, sponsored by Pfizer.

Completed
Registry status
Phase 3
Development phase
896
Enrollment target

NCT00536484: Completed Phase 3 study, sponsored by Pfizer.

NCT00536484 is a Phase 3 study that has completed, run by Pfizer. The registered enrollment target is 896 participants, above the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (16% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00536484, a Phase 3 study, has completed, sponsored by Pfizer.

COMPLETED
Registry status
Phase 3
Development phase
896 participants
Enrollment target

Study Summary

This Phase 3B study is designed to test if a fesoterodine flexible dose regimen is more effective than placebo in reducing micturition frequency and other overactive bladder (OAB) symptoms, e.g., urgency, urgency incontinence episodes in patients with overactive bladder and if the fesoterodine regimen is safe and well tolerated.

Primary Outcome

The number of micturitions per 24 hours was calculated as the sum of all micturitions divided by the total number of diary days collected at that visit. Change: mean at Week 12 minus mean at Baseline

Interventions

  • DRUG Placebo
  • DRUG Fesoterodine

Trial Details

FieldValue
Enrollment Target 896 participants
Start Date 2007-08
Est. Completion 2008-03
Phase Phase 3
Pfizer

1,845 total trials

What the finished NCT00536484 record still lists

NCT00536484 is an interventional study that assigns participants to a tested intervention. The registered 896 participants enrollment target is mid-sized for trials with a published cap, above the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (16% higher).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT00536484 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00536484 about?

NCT00536484 is a clinical study titled "Fesoterodine Flexible Dose Study". This Phase 3B study is designed to test if a fesoterodine flexible dose regimen is more effective than placebo in reducing micturition frequency and other overactive bladder (OAB) symptoms, e.g., urgency, urgency incontinence episodes in patients with overactive bladder and if the fesoterodine regim...

What is the current status of trial NCT00536484?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 896 participants. The study started on 2007-08. Estimated completion is 2008-03.

What interventions are being tested in trial NCT00536484?

The interventions under investigation include: Placebo (DRUG), Fesoterodine (DRUG).

Who is sponsoring clinical trial NCT00536484?

This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00536484's enrollment target sits among peer trials

896 361st of 2000 higher than 1,640 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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 NCT00536484, the US trial registry maintained by the National Library of Medicine. NCT00536484 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.