drugset / Trial / NCT07206706

Efficacy and Tolerability of Tadalafil Versus Darifenacin in Management of Ureteric Stent-Related LUTS

NCT07206706

Phase 1/2 Completed 150 enrolled Ain Shams University
RandomizedCrossoverSingle-blindTreatment

Summary

This randomized, crossover clinical trial evaluated the efficacy and safety of tadalafil compared with darifenacin in managing lower urinary tract symptoms (LUTS) and pain related to indwelling ureteric stents. A total of 150 patients who underwent ureteric stent insertion after endoscopic treatment of ureteric stones were enrolled. Patients were randomized into two groups: Group 1 received tadalafil 5 mg once daily for 3 weeks, followed by a 1-week washout, then darifenacin 7.5 mg once daily for 3 weeks. Group 2 received the reverse sequence. The primary outcome was change in LUTS as measured by a shortened International Prostate Symptom Score (IPSS). The secondary outcome was stent-related pain measured by the Numeric Pain Rating Scale (NPRS). Drug safety and tolerability were also assessed.

Timeline

Start
2022-05-01
Primary completion
2022-12-14
Completion
2022-12-28

Drugs

EvaluationDrugModalityDoseRoute
Subject Darifenacin Small molecule 7.5 mg Oral
Subject Tadalafil Small molecule 5 mg Oral

Indications

No indication recorded.