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NCT00212264 · ClinicalTrials.gov registry record · NA
Conservative Treatment of Postprostatectomy Incontinence
A NA study, sponsored by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK).
- Completed
- Registry status
- NA
- Development phase
- 208
- Enrollment target
NCT00212264: Completed NA study, sponsored by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK).
NCT00212264 is a NA study that has completed, run by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK). The registered enrollment target is 208 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (85% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00212264, a NA study, has completed, sponsored by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK).
- COMPLETED
- Registry status
- NA
- Development phase
- 208 participants
- Enrollment target
Study Summary
The primary purpose of this study is to test the effectiveness, impact on quality of life, and durability of non-surgical therapies for incontinence persisting at least one year after surgery. The study is a a prospective, controlled, randomized trial comparing an 8-week, multi-component behavioral training program (pelvic floor muscle exercises, self-monitoring with bladder diaries, regular office visits, bladder control techniques, and fluid management) to the same program with the addition of biofeedback and pelvic muscle electrical stimulation.
Primary Outcome
\[(Baseline incontinence episodes minus 2-month incontinence episodes)/baseline incontinence episodes\] x 100%
Interventions
- BEHAVIORAL Biofeedback
- OTHER No Treatment
- BEHAVIORAL Behavioral Therapy
- DEVICE Pelvic Floor Electrical Stimulation
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 208 participants |
| Start Date | 2003-08 |
| Est. Completion | 2011-08 |
| Phase | NA |
What the finished NCT00212264 record still lists
NCT00212264 is an interventional study that assigns participants to a tested intervention. The registered 208 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (85% lower).
The record links to 0 conditions, and to 4 interventions - of which Biofeedback is the first listed.
NCT00212264 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00212264 about?
NCT00212264 is a clinical study titled "Conservative Treatment of Postprostatectomy Incontinence". The primary purpose of this study is to test the effectiveness, impact on quality of life, and durability of non-surgical therapies for incontinence persisting at least one year after surgery. The study is a a prospective, controlled, randomized trial comparing an 8-week, multi-component behavioral ...
What is the current status of trial NCT00212264?
This trial is currently completed. It is a NA study. The enrollment target is 208 participants. The study started on 2003-08. Estimated completion is 2011-08.
What interventions are being tested in trial NCT00212264?
The interventions under investigation include: Biofeedback (BEHAVIORAL), No Treatment (OTHER), Behavioral Therapy (BEHAVIORAL), Pelvic Floor Electrical Stimulation (DEVICE).
Who is sponsoring clinical trial NCT00212264?
This trial is sponsored by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), which has 490 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00212264's enrollment target sits among peer trials
208 496th of 2000 higher than 1,502 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA 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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