Prospective Trial Comparing Oxybutynin and Tamsulosin for Stent Pain in the Pediatric Population
Status:
Unknown status
Trial end date:
2016-12-01
Target enrollment:
Participant gender:
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.