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NEUROTOX: Two Dosages of Type A Botulinic Toxin in Neurogenic Overactive Bladder

Overactive Bladder Clinical Trial

Official title:
Evaluation of the Efficacy and Tolerance of 2 Dosages of Type A Botulinic Toxin in Neurogenic Areactive Bladder Resistant to Oral Medical Treatment

Clinical Trial Summary

The purpose of this study is to determine the efficacy and tolerance of 2 dosages (750 versus 500 units) of the Dysport type A botulinic toxin for patient suffering from neurogenic urinary incontinence by an overactive bladder and the failure of anticholinergic drugs.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00213577
Study type Interventional
Source University Hospital, Rouen
Contact
Status Terminated
Phase Phase 2
Start date December 2003
Completion date October 2007
View Details
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