Clinical trial

Safety and Efficacy Study of Transdermal Oxybutynin to Treat Overactive Bladder…

NCT00224016 · Watson Pharmaceuticals, Industry · Completed

Key facts

NCT number NCT00224016
Title Safety and Efficacy Study of Transdermal Oxybutynin to Treat Overactive Bladder With a Neurological Condition
Official title A Multi-Center, Open-Label (OL), Active-Controlled, Dose-Titration Study Evaluating the Safety, Efficacy and PK of Oxybutynin Transdermal Systems in the Treatment of Detrusor Overactivity in Pediatric Patients
Lead sponsor Watson Pharmaceuticals, Industry
Status Completed
Phase Phase 4
Study type Interventional
Conditions Detrusor Hyperreflexia
Intervention type Drug
Interventions Oxybutynin
Enrollment 57
Start date Dec 1, 2004
Primary completion Apr 1, 2007
Completion Sep 1, 2008
First posted Sep 22, 2005
Last update posted Feb 9, 2012
Countries United States

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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