Mixed Urinary Incontinence Surgical Trial

NCT ID: NCT03085979

Last Updated: 2022-07-27

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

Clinical Phase

NA

Total Enrollment

198 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-10-31

Study Completion Date

2022-05-31

Brief Summary

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Surgical management of mixed urinary incontinence

Detailed Description

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Study to evaluate role of anti-incontinent surgery Burch colposuspension Tension free vaginal tape Trans obturator tape for the management of mixed urinary incontinence .

Conditions

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Med: Urinary Incontinence (Stress, Urge, Mixed)

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Burch

Burch Colposuspension

Group Type EXPERIMENTAL

Burch Colposuspension

Intervention Type PROCEDURE

Anti-incontinent surgery

Trans Obturator Tape

Trans Obturator Tape sling

Group Type EXPERIMENTAL

trans obturator tape

Intervention Type PROCEDURE

Anti-incontinent surgery

Tension free vaginal tape

Tension free vaginal tape sling

Group Type EXPERIMENTAL

tension free vaginal tape

Intervention Type PROCEDURE

Anti-incontinent surgery

Interventions

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Burch Colposuspension

Anti-incontinent surgery

Intervention Type PROCEDURE

trans obturator tape

Anti-incontinent surgery

Intervention Type PROCEDURE

tension free vaginal tape

Anti-incontinent surgery

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* patients with Mixed urinary incontinence

Exclusion Criteria

Women with associated gynecological surgery e.g. uterine prolapse, previous anti-incontinence surgery, intrinsic sphincter deficiency (ISD), and medical disorders affecting the bladder innervation as diabetes mellitus were excluded from the study. Women who improved on medical treatment with persistence of stress element only were also excluded.
Minimum Eligible Age

20 Years

Maximum Eligible Age

60 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Ain Shams Maternity Hospital

OTHER

Sponsor Role lead

Responsible Party

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Hamdy Ahmed Saaid

Fellow of OBSlGYN

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Hamdy HA Ahmed Saaid, M.D

Role: PRINCIPAL_INVESTIGATOR

Fellow of OBS/GYN

Other Identifiers

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MUIT

Identifier Type: -

Identifier Source: org_study_id

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