Clinical Trials Directory

Trials / Unknown

UnknownNCT06334848

Efficacy of Mini Sling Versus Transobturator Tape in Surgical Management of Women With Stress Urinary Incontinence

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
42 (estimated)
Sponsor
Ain Shams University · Academic / Other
Sex
Female
Age
60 Years
Healthy volunteers
Accepted

Summary

To compare the efficacy of mini sling against Transobturator tape for surgical management of women with stress urinary incontinence.

Detailed description

Urinary incontinence is defined as involuntary loss of urine and is divided into subtypes according to symptoms. These subtypes include SUI, in which urine loss occurs during exertion, physical exercise, coughing or sneezing; urgency urinary incontinence (UUI), in which urine loss is associated with urinary urgency; and mixed urinary incontinence (MUI), which is characterized by the association of stress loss with urgency. There are non-surgical treatments (e.g., lifestyle modifications, pharmacotherapy, physiotherapy and vaginal pessary) and surgical treatments. As regards sling use, it was found that mid urethral slings techniques achieved high cure rates in women with SUI and have become the mainstay for surgical treatment of SUI in women over the last 2 decades. One of the modalities of such procedures is the transobturator mid urethral tape (TOT). It was introduced to minimize the complications of the previous retropubic tapes, which include injury to the bladder, major vessels, and bowel. In an effort to maintain efficacy while eliminating some of the side effects, a new generation of tapes has been developed, called single incision tapes or mini-slings. They are designed to be shorter in length than standard mid-urethral slings and do not penetrate the tissues as deeply as standard slings.

Conditions

Interventions

TypeNameDescription
PROCEDUREtransobturator tapeWomen with stress urinary incontinence are treated by transobturator tape versus mini sling

Timeline

Start date
2024-04-01
Primary completion
2025-04-01
Completion
2025-09-01
First posted
2024-03-28
Last updated
2024-03-28

Source: ClinicalTrials.gov record NCT06334848. Inclusion in this directory is not an endorsement.