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Recruiting Phase 2

Tamsulosin and Intraureteral Aminophylline for Ureteral Access During RIRS

NCT07623876 · tracked via the Priya Life Science Egypt tracker
Phase
Phase 2
Started
2026-05-06
Last updated
2026-06-03

Condition(s) studied

Renal StonesRetrograde Intrarenal SurgeryUreteral Access Sheath Placement

Investigational drug(s) / intervention(s)

Tamsulosin →Placebo CapsuleIntraureteral AminophyllineIntraureteral Placebo

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

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age 18 years or older. * Unilateral renal stone 2 cm or less in maximal diameter on preoperative imaging. * Scheduled for primary retrograde intrarenal surgery. * Ability to provide written informed consent. Exclusion Criteria: * Prior ureteral stenting on the study side. * Bilateral same-session retrograde intrarenal surgery. * Concomitant ureteral stone requiring primary semirigid ureteroscopy as the main procedure. * Known ureteral stricture or prior ureteral reconstructive surgery on the study side. * Active urinary tract infection or untreated positive urine culture. * Pregnancy. * Known allergy or contraindication to tamsulosin or aminophylline. * Significant cardiac arrhythmia, uncontrolled ischemic heart disease, seizure disorder, or hyperthyroidism. * Severe hepatic impairment. * Inability to comply with the 7-day preoperative medication protocol.

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)

FacilityCityRegionStatus
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
Official registry record

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