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Title   A P3, rando'd, dbl-blind, parallel-group, placebo-cont'd study to assess efficacy & safety of 1 or more intradetrusor tx of 600 or 800 units of Dysport for tx of urinary incontinence in subjects w/neurogenic detrusor overactivity d/t spinal injury or MS
Disease/Condition   Wound Infection and Healing,Urinary Disorders,Urologic Diseases,Multiple Sclerosis,Incontinence,Autoimmune Diseases,Spinal Cord Diseases
Description  

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Eligibility Criteria   Click here for eligibility requirements
Principal Investigator   Nitya Abraham, MD
Contact Name   JoAnn Horn
Contact Email   Johor@montefiore.org
Protocol Number   17-02-90-01
Inclusion/Notes   This information was obtained from ClinicalTrials.gov.
Status   Active/Enrolling
Adult Clinical Trial   Yes
Pediatric Clinical Trial   No