Clinical Trials Directory

Trials / Completed

CompletedNCT02010788

Evaluation of Safety and Efficacy of Botulinum Toxin Type A (BOTOX®) to Treat Urinary Incontinence Due to Neurogenic Detrusor Overactivity or Overactive Bladder in Korea

Status
Completed
Phase
Study type
Observational
Enrollment
523 (actual)
Sponsor
Allergan · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study is a Post-Marketing Surveillance study in Korea to evaluate the safety and efficacy of botulinum toxin Type A to treat urinary incontinence in patients with neurogenic detrusor overactivity (NDO) or overactive bladder (OAB) not adequately controlled by anticholinergic drugs.

Conditions

Interventions

TypeNameDescription
BIOLOGICALbotulinum toxin Type ABotulinum toxin Type A treatment for Neurogenic Detrusor Overactivity or Overactive Bladder as per local standard of care in clinical practice.

Timeline

Start date
2014-02-01
Primary completion
2016-07-01
Completion
2016-07-01
First posted
2013-12-13
Last updated
2016-09-22

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT02010788. Inclusion in this directory is not an endorsement.

Evaluation of Safety and Efficacy of Botulinum Toxin Type A (BOTOX®) to Treat Urinary Incontinence Due to Neurogenic Det (NCT02010788) · Clinical Trials Directory