Clinical Trials Directory

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:

21 Years - N/A

Inclusion Criteria

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

External Links

Contact information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Tine Bjornlund

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