Observing Pelvic Organ Prolapse Symptoms And Treatment Outcomes

Status Terminated

Clinical Trial 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.

Clinical Trial Description

Patients meeting the inclusion/exclusion criteria will be identified by reviewing the hospital's surgical boarding list and contacted by phone to obtain informed consent. Once informed consent is obtained, chart review will be conducted here at William Beaumont Hospital and at the physician's office to collect patient information related to their prolapse condition. Prior to surgery, questionnaires will be mailed and completed by the participant and then again at 6 and 12 months after surgery, and then yearly. Questionnaires will assess urinary, bowel, and sexual function, and patient treatment goals, treatment satisfaction, and general health and wellbeing. Completion of the questionnaires will be voluntary, and participants will be followed in this manner until voluntary withdrawal, exclusionary criteria emerge, or death. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00784602
Study type	Observational
Source	William Beaumont Hospitals
Contact
Status	Terminated
Phase	N/A
Start date	October 29, 2008
Completion date	August 29, 2016

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See also
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