Observing Pelvic Organ Prolapse Symptoms And Treatment Outcomes
| Status: | Terminated |
|---|---|
| Conditions: | Women's Studies |
| Therapuetic Areas: | Reproductive |
| Healthy: | No |
| Age Range: | 21 - Any |
| Updated: | 1/5/2018 |
| Start Date: | October 29, 2008 |
| End Date: | August 29, 2016 |
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.
bowel, and sexual function, quality of life, patient satisfaction, cost, and achieving
patient determined treatment goals.
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.
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.
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
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