drugset / Trial / NCT00224029

A Study Evaluating Oxybutynin in Patients With Neurogenic Overactive Bladder Associated With a Neurological Condition

NCT00224029

Phase 4 Completed 24 enrolled Watson Pharmaceuticals
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This study will evaluate the efficacy and safety of an anticholinergic drug treatment administered by transdermal patch to treat overactive bladder in adults who have spinal cord injury.

Timeline

Start
2004-12
Primary completion
2005-12
Completion
2008-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Oxybutynin Small molecule 3.9 mg Other
Subject Oxybutynin Small molecule 7.8 mg Other
Subject Oxybutynin Small molecule 9.1 mg Other
Subject Oxybutynin Small molecule 11.7 mg Other

Indications