Tamsulosin and Intraureteral Aminophylline for Ureteral Access During RIRS
Condition(s) studied
Investigational drug(s) / intervention(s)
Tamsulosin: Tamsulosin 0.4 mg capsule once daily for 7 days before retrograde intrarenal surgery.
Placebo Capsule: Matching placebo capsule for tamsulosin, taken once daily for 7 days before retrograde intrarenal surgery.
Intraureteral Aminophylline: Aminophylline 250 mg/10 mL will be diluted with 10 mL normal saline 0.9% to a total volume of 20 mL. The solution will be instilled intraureterally through an open-end ureteric catheter positioned in the distal ureter on the study side. After a standardized 5-minute waiting period, one controlled attempt will be made to place the planned 10/12 Fr ureteral access sheath.
Intraureteral Placebo: Normal saline 0.9% to a total volume of 20 mL will be instilled intraureterally through an open-end ureteric catheter positioned in the distal ureter on the study side. After a standardized 5-minute waiting period, one controlled attempt will be made to place the planned 10/12 Fr ureteral access sheath.
Study summary
This multicenter randomized controlled trial will evaluate whether preoperative tamsulosin, intraureteral aminophylline, or their combination can improve ureteral access during primary retrograde intrarenal surgery for renal stones. Adult patients with unilateral renal stones measuring 2 cm or less and planned placement of a 10/12 Fr ureteral access sheath will be randomly assigned to one of four groups in a 2x2 factorial design. Participants will receive either tamsulosin or placebo for 7 days before surgery and either intraureteral aminophylline or intraureteral placebo during the procedure. The main outcome will be successful first-attempt placement of the planned 10/12 Fr ureteral access sheath after study solution instillation, without active ureteral dilatation, sheath downsizing, prestenting with deferred surgery, or abandonment of the procedure due to access failure.
Eligibility
Primary outcome measure(s)
- Successful First-Attempt 10/12 Fr Ureteral Access Sheath Placement — During the index retrograde intrarenal surgery procedure
Successful placement of the planned 10/12 Fr ureteral access sheath at the first standardized post-instillation attempt during primary retrograde intrarenal surgery, without active ureteral dilatation, sheath downsizing, prestenting with deferred retrograde intrarenal surgery, or abandonment of the procedure due to access failure.
Trial sites (3)
| Facility | City | Region | Status |
|---|---|---|---|
| Department of Urology- Aswan University Hospitals | Aswān | Aswan Governorate | Recruiting |
| Department of Urology- Beni-Suef University Hospitals | Banī Suwayf | Beni Suweif Governorate | Recruiting |
| Urology Department- Sohag university Hospital | Sohag | Sohag Governorate | Recruiting |
On this site
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Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07623876 on ClinicalTrials.gov ↗ ← All trials in Egypt