Long Term Outcome Women Who Undergone Mid-urethral Sling Surgery

Long Term Outcome Women Who Undergone Mid-urethral Sling Surgery Using Urogynecologic Ultrasonographic and Urodynamic Evaluation

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT03831217

Enrollment

Registered

2019-02-05

Start date

2019-10-15

Completion date

2020-06-15

Last updated

2023-04-26

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

Conditions

Stress Urinary Incontinence

Keywords

Trans-Obturator Tape, Tension-Free Vaginal Tape, Mid-Urethral Sling surgeries, Stress Urinary Incontinence

Brief summary

The patients who underwent mid-urethral sling surgery for stress urinary incontinence will evaluate. The aim of our study is to assess long term surgical outcomes and post operative clinical findings include physical examinations, quality of life questionnaires, ultrasonographic measurements.

Detailed description

Patients who underwent mid-urethral sling surgery in Ankara University Obstetrics and Gynecology Department since 2007 will be included. Primary outcome measure is to describe factors effecting long term success in mid-urethral sling surgery.

Interventions

PROCEDUREmid urethral sling surgery

patients with clinically and/or urodynamically proven stress urinary incontinence underwent mid urethral sling surgery under general anesthesia.

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

FEMALE

Inclusion criteria

* Undergoing surgery in Ankara University Obstetrics and Gynecology Department since 2007 * Patients come to follow up

Exclusion criteria

* inability in verbal and written communication * impairment in cognitive functions

Design outcomes

Primary

Measure	Time frame	Description
Objective cure rates	1-11 years	Objective cure is negative cough stress test.
Subjective cure rates	1-11 years	Subjective cure is evaluated with PGI-I instrument. Patients who give 'much better' or 'better' response to the PGI question are considered subjectively cured.

Secondary

Measure	Time frame	Description
Tape localization	1-11 years	Length of urethra, length of mesh, distance between urethra and mesh, distance between mesh and bladder neck will be measured. The correlation between these parameters and surgical success will be evaluated
Quality of life(QoL) after surgery	1-11 years	Impact of surgery on quality of life will be evaluated by QoL questionnaire
Patient satisfaction	1-11 years	Patient satisfaction will be assessed using a 10-points Visual Analogue Scale (VAS) that ranged from ''complete achievement of my goal'' (10 points) to ''no achievement of my goal'' (0 points). Patient Global Impression of Improvement (PGI-I) and VAS scale correlation will be evaluated.

Countries

Turkey (Türkiye)

Outcome results

None listed

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