A Large Multi-Center Database of Women Who Have Had and Are Going to Have Surgical Correction of Their Pelvic Organ Prolapse Using the Gynecare Prolift System

NCT01134003 · Status: COMPLETED · Type: OBSERVATIONAL

Last updated 2010-05-31

No results posted yet for this study

Summary

retrospective and prospective data collection for a database. Patients will have had or are going to have a repair of their pelvic organ prolapse using the Gynecare mesh Prolift System

Conditions

  • Pelvic Organ Prolapse

Sponsors & Collaborators

  • The Institute of Pelvic Medicine & Reconstructive Surgery, Allentown, Pennsylvania

    lead OTHER

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-01-31
Primary Completion
2009-11-30
Completion
2009-12-31

Countries

  • United States

Study Locations

More Related Trials

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 NCT01134003 on ClinicalTrials.gov