Study of Silodosin to Facilitate Passage of Urinary Stones

Status Completed

Clinical Trial Summary

The purpose of this study is to assess if patients treated with silodosin will have a higher spontaneous passage rate of their ureteral stone than those treated with placebo.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01144949
Study type	Interventional
Source	Watson Pharmaceuticals
Contact
Status	Completed
Phase	Phase 2
Start date	June 2010
Completion date	July 2012

View Details

See also
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