Clinical Trials Directory

Trials / Completed

CompletedNCT01228370

Efficacy and Safety of Silodosin on Voiding Dysfunction Associated With Neurogenic Bladder

A 12-week, Open-label, Multi-center Study to Evaluate the Clinical Efficacy and Safety of Silodosin on Voiding Dysfunction Associated With Neurogenic Bladder

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
95 (actual)
Sponsor
JW Pharmaceutical · Industry
Sex
All
Age
20 Years
Healthy volunteers
Not accepted

Summary

Because the bladder neck and proximal urethra contain abundant α1-adrenergic receptors, α-blockers or α1-blockers are well-known to reduce bladder neck obstruction in patients with or without neurogenic bladder. α1-blockers seem to have a potential to reduce bladder outlet resistance during voiding in patients with neurogenic bladder. Based on these turnouts, we designed this clinical study to evaluate the clinical effect and safety of silodosin on voiding dysfunction associated with neurogenic bladder.

Conditions

Interventions

TypeNameDescription
DRUGsilodosinsilodosin 8mg once a day for 12 weeks

Timeline

Start date
2011-04-01
Primary completion
2012-01-01
Completion
2012-01-01
First posted
2010-10-26
Last updated
2012-10-05

Locations

6 sites across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01228370. Inclusion in this directory is not an endorsement.

Efficacy and Safety of Silodosin on Voiding Dysfunction Associated With Neurogenic Bladder (NCT01228370) · Clinical Trials Directory