Distal Ureteral Stone

2

Review clinical trials related to Distal Ureteral Stone. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Intravesical Aminophylline to Facilitate Ureteroscopic Access in Children With Distal Ureteral Stones.

This study will evaluate whether intravesical aminophylline can facilitate semi-rigid ureteroscopic access in children with distal ureteral stones when the first gentle attempt to enter the ureter is unsuccessful. Children scheduled for semi-rigid ureteroscopy for distal ureteral stones will first undergo the standard gentle attempt to pass the ureteroscope through the ureteric orifice and intramural ureter. If access is achieved, the child will continue standard treatment and will not be randomized. If access is not achieved, the child will be randomized during the operation to receive either intravesical aminophylline or intravesical normal saline placebo. The study solution will be instilled into the bladder for approximately 5 minutes, then drained, and a second gentle ureteroscopic access attempt will be made. The main outcome is successful same-session passage of the intended semi-rigid ureteroscope without balloon dilation. The study will also assess the need for JJ stenting and deferred ureteroscopy, same-session stone treatment, operative outcomes, complications, and early aminophylline-related safety.

Participants needed: 60
Trial details
Phase: Phase 2Age: 2-18Biological sex: AllType: InterventionalSponsor: Beni-Suef UniversityUpdated: Jun 1, 2026Locations: 1
Eligibility criteria

Children older than 2 years and younger than 18 years. [+6]

Known hypersensitivity to aminophylline, theophylline, or ethylenediamine. [+9]

Status: Recruiting

L-Citrulline Versus Tamsulosin for Medical Expulsive Therapy of Distal Ureteral Stones

This study will compare L-citrulline and tamsulosin as medical expulsive therapy for adults with single distal ureteral stones. Eligible participants with a single distal ureteral stone measuring 5 to 10 mm will be randomly assigned to receive either oral L-citrulline 750 mg twice daily or oral tamsulosin 0.4 mg once daily. Treatment will continue until documented stone passage or completion of 4 weeks of therapy, whichever occurs first. Participants will be followed weekly for up to 4 weeks. The main outcome is stone expulsion within 4 weeks. The study will also assess time to stone expulsion, pain episodes, analgesic use, need for additional intervention, and adverse events.

Participants needed: 120
Trial details
Phase: Phase 2Age: 18-60Biological sex: AllType: InterventionalSponsor: Beni-Suef UniversityUpdated: Jun 1, 2026Locations: 1
Eligibility criteria

Adults aged 18 to 60 years. [+6]

Fever or active urinary tract infection. [+8]