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Clinical Trial Summary

To evaluate the outcome of visual internal urethrotomy in treating urethral strictures in males with a holmium: yttrium-aluminium garnet (YAG) laser versus when combined with intralesional injection of paclitaxel.


Clinical Trial Description

Urethral strictures are one of the most common reasons for urological admissions. They are associated with urinary tract infections, bladder stones, fistulas, sepsis and possibly renal insufficiency. Minimally invasive surgical approaches are utilized efficiently and safely in the treatment of urethral strictures. Visualized internal urethrotomy VIU, is one of the preferred methods due to the practical and minimally invasive nature of the procedure. One of the alternative approaches is the correction of the stricture using laser energy. The aim of this prospective study is to evaluate the results of YAG laser internal urethrotomy (HIU) in primary urethral strictures versus using laser with intralesional submucosal paclitaxel injection. It is a prospective study in which patients will be recruited from the outpatient clinic of Demerdash (ain Shams university) hospital, randomized via closed envelope technique into doing VIU alone versus doing VIU with intralesional injection of paclitaxel After obtaining well informed written consent, all patients will undergo the following 1. Detailed history taking, including medical history, surgical history, and patient complaint according to international prostate symptom score (IPSS) score. A note will be made about the possible etiology of the stricture. 2. Clinical Examination including abdominal, pelvic and genital examination. 3. Laboratory investigations including complete blood count, urine analysis, urine culture and sensitivity test, renal function tests. 4. Radiological investigations including retrograde urethrogram, micturating cystourethrogram and pelvi-abdominal ultrasound. 5. Uroflowmetry Any active urinary tract infection (UTI) will be treated before surgery with appropriate antibiotics based upon sensitivity test. All patients will be followed up intraoperatively recording operative time and the need for blood transfusion, postopertively regarding haemoglobin level, total leucocytic count level and the development of fever or not. All patients will be scheduled to remove the catheter at 14 days postoperative and assessment of international prostate symptom score (IPSS) at first day of catheter removal. Three months and six months postoperative the patients will be followed up for IPSS, Uroflowmetry results and if the patient is retained (could not urinate) or his results were worse than starting results, then cystourethrogram will be asked from him to investigate the possibility of recurrence. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06123520
Study type Interventional
Source Ain Shams University
Contact
Status Completed
Phase Phase 3
Start date May 1, 2023
Completion date October 15, 2023

See also
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Enrolling by invitation NCT06192654 - Small Intestinal Submucosa Graft for Repair of Anterior Urethral Strictures N/A
Completed NCT04650347 - Holmium: YAG Versus Cold Knife Internal Urethrotomy in Management of Short Urethral Strictures Phase 2/Phase 3
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Not yet recruiting NCT05918315 - Comparison Between Two Techniques Used in Treatment of Long Anterior Urethral Stricture N/A