CI

At a glance

ClinicalIndex Comparison Record
N/AActive· 360 enrolled
Drug / intervention
Open, Robotic, or Laparoscopic +2 moreprocedure
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02676973
NCT02676973N/AActive

Three Arm Apical Suspension Trial for Post-Hysterectomy Vault Prolapse: Prospective Randomized Trial Involving Sacral Colpopexy, Transvaginal Mesh and Native Tissue Apical Repair

NICHD Pelvic Floor Disorders Network·interventional·Posted Feb 9, 2016·Updated Aug 26, 2025

In Brief

A clinical study evaluating Open, Robotic, or Laparoscopic, Transvaginal Native Tissue Repair, and 1 other intervention for Visceral Prolapse. Active but no longer recruiting, targeting 360 participants across 10 sites.

Detailed Summary

The study is a multi-center, randomized, surgical trial of women with symptomatic post-hysterectomy apical (cuff) prolapse desiring surgical treatment. This study will compare the three available surgical treatments performed in usual practice. The purpose of this study is to compare two commonly performed mesh apical repair (sacral colpopexy vs. Apical Transvaginal Mesh) and vaginal native tissue apical repairs with mesh reinforced repairs. The primary outcome is measured over time (up to 60 months) using a survival analysis approach. Participants will be followed for at least 36-months (3-years) post surgery and up to a maximum of 60-months (5-years) during the primary trial. Participants who complete the primary trial will be approached for consent for long-term follow-up as part of a study extension and will be followed up to a maximum of 120-months (10-years). The investigators hypothesize that treatment failure will not differ between vaginally and abdominally placed mesh for vault vaginal prolapse, and mesh repairs (regardless of route of implantation) will be superior to native tissue apical suspension.

Study Details

Timeline

N/AActive
201620172018201920202021202220232024202520262027
First PostedFeb 9, 2016
Enrollment StartFeb 29, 2016
Primary CompletionJul 28, 2022
Study CompletionDec 31, 2026
TodayJul 2, 2026
Enrollment to primary: 6.4 yearsPosted 10.4 years ago

Interventions

Open, Robotic, or Laparoscopicprocedure

Sacral Colpopexy is a surgery performed either through an incision in the abdomen or through several small incisions with the help of a laparoscope (a slender tube) or robot. The surgery is done with a permanent synthetic (man-made) mesh. The mesh is sutured (stitched) to the vagina and sacrum (tail bone) and is used as reinforcement. It provides additional support to weakened tissues and/or muscles.

Transvaginal Native Tissue Repairprocedure

Transvaginal Native Tissue Repair is a surgery performed with an incision through the vagina (transvaginal). The surgery is done using both permanent and absorbable sutures (stitches), to support weakened tissue and/or muscles, and attach the top of the vagina to ligaments in the pelvis (either to the sacrospinous ligament or uterosacral ligament).

Uphold™ LITEprocedure

Transvaginal Mesh Repair is a surgery performed with an incision through the vagina (transvaginal). The surgery is done with a permanent synthetic (man-made) mesh. The mesh is attached to ligaments in the pelvis and is used to reinforce natural tissue and/or muscles, which are no longer able to provide support to the vagina.