GYNECARE PROSIMA* Pelvic Floor Repair System for Pelvic Organ Prolapse

NCT00521066 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 150

Last updated 2014-05-06

No results posted yet for this study

Summary

The purpose of this study is to is to evaluate the success of the GYNECARE PROSIMA\* system in women with symptoms for pelvic organ prolapse (POP) requiring surgical correction of POP.

(\*TRADEMARK)

Conditions

  • Pelvic Organ Prolapse

Interventions

DEVICE

GYNECARE PROSIMA* Pelvic Floor Repair System

procedure for pelvic organ prolapse

Sponsors & Collaborators

  • Ethicon, Inc.

    lead INDUSTRY

Principal Investigators

  • David Robinson, M.D. · Ethicon, Inc.

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-06-30
Primary Completion
2008-10-31
Completion
2010-06-30

Countries

  • United States
  • Australia
  • Germany
  • United Kingdom

Study Locations

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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 NCT00521066 on ClinicalTrials.gov