Clinical trial

OnabotulinumtoxinA for the Treatment of Urinary Incontinence Due to Overactive…

NCT02097121 · Allergan, Industry · Terminated

Key facts

NCT number NCT02097121
Title OnabotulinumtoxinA for the Treatment of Urinary Incontinence Due to Overactive Bladder in Pediatric Patients (12 to 17)
Official title BOTOX® in the Treatment of Urinary Incontinence Due to Overactive Bladder in Patients 12 to 17 Years of Age
Lead sponsor Allergan, Industry
Status Terminated
Phase Phase 3
Study type Interventional
Conditions Urinary Incontinence, Urinary Bladder, Overactive
Intervention type Biological
Interventions BOTOX®
Enrollment 56
Start date May 23, 2014
Primary completion Feb 10, 2022
Completion Feb 10, 2022
First posted Mar 26, 2014
Last update posted Dec 28, 2022
Countries Australia, Belgium, Canada, Czechia, France, Germany, Italy, Netherlands, Norway, Poland, South Africa, United Kingdom and 1 more

At a glance

  • 10–99 Study sites
  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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