drugset / Trial / NCT02483793
Prospective Trial Comparing Oxybutynin and Tamsulosin for Stent Pain in the Pediatric Population
Withdrawn
Phoenix Children's Hospital
RandomizedParallel-groupTreatment
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
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Oxybutynin | Small molecule | 0.5 mg/kg | — |
| Comparator | Oxybutynin | Small molecule | 5 mg | — |
| Comparator | Tamsulosin | Other / unclassified | 0.4 mg | — |