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NCT00131573 · ClinicalTrials.gov registry record · Phase 3
An Implantable Microstimulator for the Chronic Treatment of Urinary Urgency-Frequency Syndrome
A Phase 3 study, sponsored by Boston Scientific Corporation.
- Completed
- Registry status
- Phase 3
- Development phase
- 118
- Enrollment target
NCT00131573: Completed Phase 3 study, sponsored by Boston Scientific Corporation.
NCT00131573 is a Phase 3 study that has completed, run by Boston Scientific Corporation. The registered enrollment target is 118 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (85% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00131573, a Phase 3 study, has completed, sponsored by Boston Scientific Corporation.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 118 participants
- Enrollment target
Study Summary
The goal of this study is to investigate the safety and effectiveness of a new implanted device designed to treat Urinary Urgency-Frequency Syndrome.
Interventions
- DEVICE bion
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 118 participants |
| Start Date | 2004-05 |
| Est. Completion | 2012-12 |
| Phase | Phase 3 |
What the finished NCT00131573 record still lists
NCT00131573 is an interventional study that assigns participants to a tested intervention. The registered 118 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 (85% lower).
The record links to 0 conditions, and to 1 intervention - of which bion is the first listed.
NCT00131573 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00131573 about?
NCT00131573 is a clinical study titled "An Implantable Microstimulator for the Chronic Treatment of Urinary Urgency-Frequency Syndrome". The goal of this study is to investigate the safety and effectiveness of a new implanted device designed to treat Urinary Urgency-Frequency Syndrome.
What is the current status of trial NCT00131573?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 118 participants. The study started on 2004-05. Estimated completion is 2012-12.
What interventions are being tested in trial NCT00131573?
The interventions under investigation include: bion (DEVICE).
Who is sponsoring clinical trial NCT00131573?
This trial is sponsored by Boston Scientific Corporation, which has 280 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00131573's enrollment target sits among peer trials
118 1641st of 2000 higher than 359 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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