TOT, TVT And Burch Colpo-Suspension for Treatment of Female Mixed Urinary Incontinence

Ain Shams University220 enrolled

Overview

This prospective interventional randomized controlled trial will recruit women with MUI scheduled for surgical treatment where patients will be randomized to either Burch colposuspension, TOT or TVT. Regular postoperative follow up will be planned for at least 2 years. The primary outcome measures will be the objective and subjective cure rates.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

220

Conditions

Treatment

Interventions

TOTPROCEDURE

70 patients

TVTPROCEDURE

70 patients

Burch ColposuspensionPROCEDURE

70 patients

Eligibility

Sex: FEMALE

Medical Language ↔ Plain English

Inclusion Criteria: * Women 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.

Locations (1)

Ain Shams University Maternity Hospital

Cairo, Egypt

Outcomes

Primary Outcomes

objective cure rate

Time frame: 2 years

subjective cure rate

Time frame: 2 years

Data from ClinicalTrials.gov

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