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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 is a Phase 4 study that has completed, run by Medstar Health Research Institute. The registered enrollment target is 65 participants.
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 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00557882
The ClinicalTrials.gov registry entry for NCT00557882 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 65 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Medstar Health Research Institute, which has 115 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which synthetic polypropylene mesh is the first listed.
NCT00557882 reports 0 study locations.
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.
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