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. Please contact Tine Bjornlund at 6507247826 for more information.

Investigator(s):

Intervention(s):

  • device : synthetic polypropylene mesh

Phase: Phase 4

Eligibility

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

Primary Contact:

Tine Bjornlund 6507247826

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

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