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NCT00557882 · ClinicalTrials.gov registry record · Phase 4
Efficacy Study of Vaginal Mesh for Anterior Prolapse
A Phase 4 study, sponsored by Medstar Health Research Institute.
- Completed
- Registry status
- Phase 4
- Development phase
- 65
- Enrollment target
NCT00557882: Completed Phase 4 study, sponsored by Medstar Health Research Institute.
NCT00557882 is a Phase 4 study that has completed, run by Medstar Health Research Institute. The registered enrollment target is 65 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (87% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00557882, a Phase 4 study, has completed, sponsored by Medstar Health Research Institute.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 65 participants
- Enrollment target
Study Summary
The primary aim of this double-blind, randomized clinical trial (RCT) is to test the hypothesis that the addition of a standardized technique of interpositional synthetic polypropylene mesh placement improves the one-year outcome of vaginal reconstructive surgery for anterior prolapse compared to traditional vaginal reconstructive surgery without mesh.
Interventions
- DEVICE synthetic polypropylene mesh
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 65 participants |
| Start Date | 2007-06 |
| Est. Completion | 2011-11 |
| Phase | Phase 4 |
What the finished NCT00557882 record still lists
NCT00557882 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 65 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (87% lower).
The record links to 0 conditions, and to 1 intervention - of which synthetic polypropylene mesh is the first listed.
NCT00557882 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00557882 about?
NCT00557882 is a clinical study titled "Efficacy Study of Vaginal Mesh for Anterior Prolapse". The primary aim of this double-blind, randomized clinical trial (RCT) is to test the hypothesis that the addition of a standardized technique of interpositional synthetic polypropylene mesh placement improves the one-year outcome of vaginal reconstructive surgery for anterior prolapse compared to tr...
What is the current status of trial NCT00557882?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 65 participants. The study started on 2007-06. Estimated completion is 2011-11.
What interventions are being tested in trial NCT00557882?
The interventions under investigation include: synthetic polypropylene mesh (DEVICE).
Who is sponsoring clinical trial NCT00557882?
This trial is sponsored by Medstar Health Research Institute, which has 115 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00557882's enrollment target sits among peer trials
65 1091st of 2000 higher than 903 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 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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