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Detrusor Muscle Hyperactivity clinical trials

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NCT ID: NCT01357980 Completed - Clinical trials for Detrusor Muscle Hyperactivity

Neurogenic Detrusor Overactivity Following Spinal Cord Injury or Multiple Sclerosis

Start date: May 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the efficacy and safety of a single dose of 750 U of Dysport compared to placebo for the improvement in the daily incontinence episode frequency for each administration mode in subjects suffering from neurogenic detrusor overactivity following spinal cord injury or multiple sclerosis.