A Randomized Clinical Trial 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 traditional vaginal reconstructive surgery without mesh.
Stanford is now accepting new patients for this trial.
- device : synthetic polypropylene mesh
Phase: Phase 4
Ages Eligible For Study:
1. women age > 21 2. diagnosed with stage II-IV vaginal prolapse who desire reconstructive surgery 3. available for 12 months of follow-up 4. able to complete study questionnaires and assessments. 5. available for 12 months follow-up