Concomitant Posterior Colporrhaphy on Bowel Functions in Pelvic Organ Prolapse Repair

NCT ID: NCT06128291

Last Updated: 2024-10-18

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

283 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-03-03

Study Completion Date

2023-12-31

Brief Summary

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Compare the changes of preoperative and postoperative posterior colporrhaphy.

Detailed Description

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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.

Conditions

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Prolapse; Female

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

RETROSPECTIVE

Study Groups

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Posterior colporrhaphy

Medical records of women received concomitant posterior colporrhaphy for their pelvic organ prolapse repairs. Comparison will be made to compare preoperative and postoperative conditions.

posterior colporrhaphy

Intervention Type PROCEDURE

posterior colporrhaphy for rectocele.

Interventions

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posterior colporrhaphy

posterior colporrhaphy for rectocele.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

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

Exclusion Criteria

* Pregnancy
Minimum Eligible Age

20 Years

Maximum Eligible Age

100 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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National Taiwan University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Ho-Hsiung Lin, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

National Taiwan University Hospital

Locations

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National Taiwan University Hospital

Taipei, , Taiwan

Site Status

Countries

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Taiwan

Other Identifiers

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202303052RINA

Identifier Type: -

Identifier Source: org_study_id

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