Prospective Trial Comparing Oxybutynin and Tamsulosin for Stent Pain in the Pediatric Population

Summary

The primary objective of this study is to evaluate the efficacy and safety tamsulosin in reducing stent discomfort in the pediatric population in the peri-operative period. The secondary objective is to compare the efficacy of tamsulosin with that of oxybutynin in reducing stent discomfort.

Timeline

Start

2015-07

Primary completion

2016-12

Completion

2016-12

Outcome

Outcome not reported

Stopped (Enrollment): “The study was withdrawn prior to IRB approval and prior to enrollment. The study was never opened, and no participants were enrolled.”

Drugs

Indications