Outcomes and Patient Satisfaction After Colpocleisis for Pelvic Organ Prolapse

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

48 participants

Study Classification

OBSERVATIONAL

Study Start Date

2006-07-31

Study Completion Date

2009-01-31

Brief Summary

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The purpose of this study is to evaluate the long-term success rate of the colpocleisis procedure and its effect on quality of life in women who have this surgery. We want to see if women who have this surgery have problems with recurrent pelvic organ prolapse, urinary incontinence, or bowel problems after the surgery. We also want to see how the surgery affects women's sexuality.

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Detailed Description

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Conditions

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Pelvic Organ Prolapse

Study Design

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Observational Model Type

COHORT

Study Groups

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1

Physical examination, questionnaires, retrospective chart review

Questionnaires, Physical Examination

Intervention Type OTHER

Questionnaires, Physical Examination

2

Questionnaires, retrospective chart review

Questionnaires, Physical Examination

Intervention Type OTHER

Questionnaires, Physical Examination

3

Retrospective chart review

No interventions assigned to this group

Interventions

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Questionnaires, Physical Examination

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* women who underwent either total colpectomy with colpocleisis or partial colpectomy with LeFort-type colpocleisis performed by the Urogynecology service between 1/2000 and 12/2007 at Strong Memorial Hospital