Outcomes and Patient Satisfaction After Colpocleisis for Pelvic Organ Prolapse

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00714155

Enrollment

Registered

2008-07-14

Start date

2006-07-31

Completion date

2009-01-31

Last updated

2012-06-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pelvic Organ Prolapse

Keywords

Colpocleisis

Brief summary

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.

Interventions

OTHERQuestionnaires, Physical Examination

Questionnaires, Physical Examination

Study design

Observational model

COHORT

Eligibility

Sex/Gender

FEMALE

Age

18 Years to No maximum

Healthy volunteers

Yes

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

Exclusion criteria

* women who are not undergone colpocleisis or colpectomy

Design outcomes

Primary

Measure	Time frame
Questionnaires	Post-operative

Secondary

Measure	Time frame
Physical Examination	Post-operative

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026