← Eichor
Study identifier: NCT07414849 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

The AMPER Study: Evaluation of the Efficacy of Human Amniotic Membrane Grafting in Preventing Mesh Exposure in Vaginal Reconstructive Surgery Using Polypropylene Mesh.

Condition: Pelvic Organ Prolapse Vaginal Surgery · Stress Urinary Incontinence in Women  ·  Sponsor: Hospital General de Agudos J. M. Penna

PhaseNA
Planned participants330
Who can joinFemale, N/A to no upper limit
Healthy volunteersNo

About this study

This study evaluates the efficacy of adding a human amniotic membrane graft to polypropylene mesh surgery for pelvic prolapse and stress urinary incontinence. The goal is to assess improvements in tissue integration and the reduction of surgical complications

This description comes directly from the study's public registry record.

Talk to the study team

Ileana Sanger, MD  ·  5491149113030  ·  ilesaenger@me.com

Always discuss trial participation with your own doctor first.

Locations (1)

Hospital J M PennaBuenos Aires, ArgentinaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07414849