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NCT02590250

A Safety and Efficacy Study of BOTOX® (Botulinum Toxin Type A) in Patients With Urinary Incontinence Due to Neurogenic Detrusor Overactivity or Overactive Bladder in India

Completed Last updated 26 March 2018
What this trial tests

trial testing botulinum toxin Type A in Urinary Incontinence in 250 participants. Completed in 7 August 2017.

Timeline
16 December 2015
Primary endpoint
7 August 2017
7 August 2017

Quick facts

Lead sponsorAllergan
StatusCompleted
Study typeOBSERVATIONAL
Enrollment250
Start date16 December 2015
Primary completion7 August 2017
Estimated completion7 August 2017
Sites12 locations across India

Drugs / interventions tested

Conditions studied

Sponsor

Allergan — full company profile →

Who can join

18 and older, any sex, with Urinary Incontinence or Overactive Bladder. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a Post-Marketing Surveillance study in India to evaluate safety and efficacy of BOTOX® (Botulinum Toxin Type A) in the treatment of patients with urinary incontinence due to neurogenic detrusor overactivity or overactive bladder.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of botulinum toxin Type A

Trials testing the same drug.

Other recruiting trials for Urinary Incontinence

Currently open trials in the same condition.

Other Allergan trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02590250.

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