Naftopidil 75mg for Improving Clearance of Urinary Stones

Status Not yet recruiting

Clinical Trial Summary

The purpose of this study is to evaluate Efficacy and Safety of oral intake of Naftopidil 75mg once daily for the improving clearance of ureteral or renal stones.

Clinical Trial Description

Prospective, Single-center, Double blind, Randomized controlled trial

Treatment

- Oral Naftopidil 75 mg once daily are given to the patients who are scheduled for shockwave lithotripsy (ESWL) because of ureteral or renal stones.

Follow up Assessments including X-ray(KUB), visual analogue pain scale, are done 2, 4, and 6 weeks after the ESWL. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/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	NCT02011737
Study type	Interventional
Source	Samsung Medical Center
Contact	Deok Hyun Han, MD
Phone	82-2-3410-6431
Email	deokhyun.han@gmail.com
Status	Not yet recruiting
Phase	Phase 4
Start date	February 2014
Completion date	April 2015

View Details

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