Expired Study
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Royal Oak, Michigan 48073


Purpose:

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.


Study summary:

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.


Criteria:

Inclusion Criteria: - Female - Pelvic Organ Prolapse - Able to provide informed consent - Able to complete study assessments, per clinician judgment Exclusion Criteria: - Age < 21 years - Currently pregnant or < 6 months post-partum


NCT ID:

NCT00784602


Primary Contact:

Principal Investigator
Melissa Fischer, MD
William Beaumont Hospitals


Backup Contact:

N/A


Location Contact:

Royal Oak, Michigan 48073
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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