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Clinical Trial 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.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02483793
Study type Interventional
Source Phoenix Children's Hospital
Contact Michael Nguyen, MD
Phone (602) 933-5200
Email mtn1023@hotmail.com
Status Not yet recruiting
Phase N/A
Start date July 2015
Completion date December 2016

See also
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Completed NCT01959074 - The Effect of Naftopidil for the Double-J Stent Discomfort Phase 3
Completed NCT01530243 - The Effect of Terazosin and Tolterodine on Ureteral Stent Related Symptoms Phase 2/Phase 3
Active, not recruiting NCT02007980 - Indwelling Stent Discoloration Project