Stress Urinary Incontinence Clinical Trial
Official title:
Long-term Outcomes of Autologous Transobturator Rectus Fascia Sling for Treatment of Female Stress Urinary Incontinence, Prospective Trial
Verified date | December 2022 |
Source | Al-Azhar University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Autologous transobturator sling placement is associated with excellent short-term results and can be performed on an outpatient basis in most cases, so long-term outcomes needs to be verified.
Status | Recruiting |
Enrollment | 200 |
Est. completion date | January 1, 2024 |
Est. primary completion date | January 1, 2024 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | N/A and older |
Eligibility | Inclusion Criteria: - Women with genuine stress urinary incontinence. - Mixed urinary incontinence with predominant stress element. - Refractory cases to conservative therapy or patients who are not willing to consider (further) conservative treatment. Exclusion Criteria: - Mild Stress urinary incontinence with improvement on conservative therapy or patients refusing surgical treatment. - Mixed incontinence with predominant Urge urinary incontinence. - Associated local abnormalities (e.g. cystocele). - Recent or active urinary tract infection. - Recent pelvic surgery. - Neurogenic lower urinary tract dysfunction. - Previous surgery for stress urinary incontinence. - Pregnancy - Less than 12 months post-partum. - Other gynaecologic pathologies affecting bladder functions ( eg,large fibroids) - Genito-urinary malignancy. - Current chemo or radiation therapy. |
Country | Name | City | State |
---|---|---|---|
Egypt | Mohamed Fawzy Salman | Cairo | |
Egypt | Urology department - Alazhar university | Cairo |
Lead Sponsor | Collaborator |
---|---|
Al-Azhar University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Complete cure OR improvement of SUI | Complete cure means no leak on cough stress test and the patient in satisfied on "patient reported outcome".
Improvement means patient reported leakage only with severe exertion and using a smaller number of pads per day and she feels that she has improved. On examination there was no stress urinary incontinence. Failure is considered when patients not fulfilling these criteria |
one year | |
Secondary | Complications of Autologous TOT | Measured by clavien-Dindo scoring system | one year | |
Secondary | Estimated blood loss | Blood loss will be estimated by counting up the gauzes and towels used during the procedure [fully soaked gauze = 50 ml blood loss; half-soaked gauze = 30 ml blood loss; fully soaked towel = 150 ml blood loss; half-soaked towel = 75 ml blood loss] (Shorn, 2009). | 24 hours | |
Secondary | Operative time | time consumption from induction of anesthesia till closure of vaginal mucosa | 2 hours |
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