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NCT00506116 · ClinicalTrials.gov registry record · Phase 3
Promoting Effective Recovery From Labor Urinary Incontinence (PERL)
A Phase 3 study, sponsored by University of Michigan.
- Completed
- Registry status
- Phase 3
- Development phase
- 140
- Enrollment target
NCT00506116 is a Phase 3 study that has completed, run by University of Michigan. The registered enrollment target is 140 participants.
The verdict
NCT00506116, a Phase 3 study, has completed, sponsored by University of Michigan.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 140 participants
- Enrollment target
Study Summary
The purpose of this study is to determine whether pushing during labor that is controlled by the woman results in less birth-related injury and less postpartum urinary incontinence (UI).
Interventions
- BEHAVIORAL Videotape, routine care, PME instruction
- BEHAVIORAL PME practice and record keeping (in diaries)
- BEHAVIORAL Non-directed or directed,spontaneous or sustained pushing
- PROCEDURE Data collection
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 140 participants |
| Start Date | 1996-07 |
| Est. Completion | 2006-12 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00506116
The ClinicalTrials.gov registry entry for NCT00506116 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 140 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Michigan, which has 1,327 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 4 interventions - of which Videotape, routine care, PME instruction is the first listed.
NCT00506116 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00506116 about?
NCT00506116 is a clinical study titled "Promoting Effective Recovery From Labor Urinary Incontinence (PERL)". The purpose of this study is to determine whether pushing during labor that is controlled by the woman results in less birth-related injury and less postpartum urinary incontinence (UI).
What is the current status of trial NCT00506116?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 140 participants. The study started on 1996-07. Estimated completion is 2006-12.
What interventions are being tested in trial NCT00506116?
The interventions under investigation include: Videotape, routine care, PME instruction (BEHAVIORAL), PME practice and record keeping (in diaries) (BEHAVIORAL), Non-directed or directed,spontaneous or sustained pushing (BEHAVIORAL), Data collection (PROCEDURE).
Who is sponsoring clinical trial NCT00506116?
This trial is sponsored by University of Michigan, which has 1,327 total clinical trials registered on ClinicalTrials.gov.
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