Observing Pelvic Organ Prolapse Symptoms And Treatment Outcomes

NCT00784602 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 301

Last updated 2018-01-03

No results posted yet for this study

Summary

To prospectively observe the outcomes of surgical prolapse treatment in terms of urinary, bowel, and sexual function, quality of life, patient satisfaction, cost, and achieving patient determined treatment goals.

Conditions

  • Genital Prolapse

Sponsors & Collaborators

  • William Beaumont Hospitals

    collaborator OTHER
  • Melissa Fischer, MD

    lead OTHER

Principal Investigators

  • Melissa Fischer, MD · William Beaumont Hospitals

Eligibility

Min Age
21 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-10-29
Primary Completion
2016-08-29
Completion
2016-08-29

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 NCT00784602 on ClinicalTrials.gov