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NCT01557244 · ClinicalTrials.gov registry record · Phase 3

A Study To Find Out How Fesoterodine Works In Children Aged 6 To 17 Years With Bladder Overactivity Caused By A Neurological Condition

A Phase 3 study, sponsored by Pfizer.

Completed
Registry status
Phase 3
Development phase
181
Enrollment target

NCT01557244: Completed Phase 3 study, sponsored by Pfizer.

NCT01557244 is a Phase 3 study that has completed, run by Pfizer. The registered enrollment target is 181 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (77% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01557244, a Phase 3 study, has completed, sponsored by Pfizer.

COMPLETED
Registry status
Phase 3
Development phase
181 participants
Enrollment target

Study Summary

The objective of the study is to find out if the medicine fesoterodine is a useful treatment in children with bladder muscle overactivity caused by a neurological condition. Children will be aged 6 to 17 years old. This is done by finding out how well it works, what the body does to fesoterodine, what side effects are experienced and the safety of fesoterodine. It will be compared with the medicine oxybutynin, which is already available for treating the condition.

Primary Outcome

Maximum cystometric bladder capacity (in milliliter) was defined as maximal tolerable cystometric capacity, until voiding or leaking begins or at a pressure of \>=40 centimeter (cm) water (H2O).

Interventions

  • DRUG Oxybutynin
  • DRUG Fesoterodine PR 4 mg
  • DRUG Fesoterodine PR 8 mg
  • DRUG Fesoterodine PR

Trial Details

FieldValue
Enrollment Target 181 participants
Start Date 2012-07-02
Est. Completion 2020-02-13
Phase Phase 3
Pfizer

1,845 total trials

What the finished NCT01557244 record still lists

NCT01557244 is an interventional study that assigns participants to a tested intervention. The registered 181 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (77% lower).

The record links to 0 conditions, and to 4 interventions - of which Oxybutynin is the first listed.

NCT01557244 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01557244 about?

NCT01557244 is a clinical study titled "A Study To Find Out How Fesoterodine Works In Children Aged 6 To 17 Years With Bladder Overactivity Caused By A Neurological Condition". The objective of the study is to find out if the medicine fesoterodine is a useful treatment in children with bladder muscle overactivity caused by a neurological condition. Children will be aged 6 to 17 years old. This is done by finding out how well it works, what the body does to fesoterodine, wh...

What is the current status of trial NCT01557244?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 181 participants. The study started on 2012-07-02. Estimated completion is 2020-02-13.

What interventions are being tested in trial NCT01557244?

The interventions under investigation include: Oxybutynin (DRUG), Fesoterodine PR 4 mg (DRUG), Fesoterodine PR 8 mg (DRUG), Fesoterodine PR (DRUG).

Who is sponsoring clinical trial NCT01557244?

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 NCT01557244's enrollment target sits among peer trials

181 1422nd of 2000 higher than 579 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 NCT01557244, the US trial registry maintained by the National Library of Medicine. NCT01557244 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.