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Concomitant Posterior Colporrhaphy on Bowel Functions in Pelvic Organ Prolapse Repair

The Impact of Concomitant Posterior Colporrhaphy on Bowel Functions in Women Who Received Pelvic Organ Prolapse Repair

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06128291
Enrollment
283
Registered
2023-11-13
Start date
2023-03-03
Completion date
2023-12-31
Last updated
2024-10-18

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

Conditions

Prolapse; Female

Brief summary

Compare the changes of preoperative and postoperative posterior colporrhaphy.

Detailed description

Introduction: Concomitant posterior colporrhaphy was frequently used during pelvic organ prolapse repair. Objectives: To evaluate the correlation between the presence of bowel symptoms and s rectocele severity and elucidate the impact of posterior colporrhaphy on bowel functions. Methods: Medical records of all consecutive women who received concomitant posterior colporrhaphy for their pelvic organ prolapse repairs were reviewed. In general, all women were requested to answer bowel incontinence assessment questionnaires before and after surgery. Possible results: Differences in rectocele severities between the presence or absence of fecal incontinence, flatus incontinence, constipation, diarrhea or sensation of residual stool will be shown.

Interventions

PROCEDUREposterior colporrhaphy

posterior colporrhaphy for rectocele.

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* women with pelvic organ prolapse planned to receive concomitant posterior colporrhaphy

Exclusion criteria

* Pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Number of participants with fecal incontinencebefore the operation, postoperative one month and three months.Number of participants present the symptom
Number of participants with flatusbefore the operation, postoperative one month and three months.Number of patients present the symptom
Number of participants with constipationbefore the operation, postoperative one month and three months.Number of patients present the symptom
Number of participants with diarrheabefore the operation, postoperative one month and three months.Number of patients present the symptom
Number of participants with sensation of residual stoolbefore the operation, postoperative one month and three months.Number of patients present the symptom

Countries

Taiwan

Outcome results

None listed

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