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Comparison of Single Versus Multicenter Outcomes for Pelvic Organ Prolapse Repair Using a Mesh-capturing Device

NCT03077490 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 319

Last updated 2019-10-23

No results posted yet for this study

Summary

Comparison of single versus multicenter outcomes for pelvic organ prolapse repair using a mesh-capturing device (The Uphold™ Vaginal Support System for apical and vaginal wall prolapse - Boston Scientific). 1-2 years follow up study comprison of 112 vs 207 patients.

Conditions

  • Prolapse Genital

Interventions

DEVICE

Transvaginal mesh Uphold TM Vaginal Support System

DEVICE

Transvaginal mesh Uphold TM Vaginal Support System.

Sponsors & Collaborators

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-03-04
Primary Completion
2016-03-30
Completion
2017-02-01
FDA Device
Yes

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03077490 on ClinicalTrials.gov