Multiple Sclerosis Clinical Trial

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Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Neurogenic Overactive Bladder

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Summary

The purpose of this study is to assess the safety and effectiveness of botulinum toxin type A in treating overactive bladder in spinal cord injury or multiple sclerosis patients.

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Eligibility Criteria

Inclusion Criteria:

Urinary incontinence as a result of neurogenic overactive bladder due to spinal cord injury or multiple sclerosis
Inadequate response to anticholinergic medication used to treat overactive bladder

Exclusion Criteria:

History of evidence of pelvic or urologic abnormality
Previous or current diagnosis of bladder or prostate cancer
Urinary tract infection at time of enrollment

Study is for people with:

Multiple Sclerosis

Phase:

Phase 3

Estimated Enrollment:

416

Study ID:

NCT00311376

Recruitment Status:

Completed

Sponsor:

Allergan

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There is 1 Location for this study

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Royal Oak Michigan, , United States

Randwick New South Wales, , Australia

Innsbruck , , Austria

Gent , , Belgium

Sherbrooke , , Canada

Ostrava , , Czech Republic

Garches , , France

Halle (Saale) , , Germany

Christchurch , , New Zealand

Wroclaw , , Poland

Moscow , , Russian Federation

Martin , , Slovakia

Lviv , , Ukraine

London , , United Kingdom

How clear is this clinincal trial information?

Study is for people with:

Multiple Sclerosis

Phase:

Phase 3

Estimated Enrollment:

416

Study ID:

NCT00311376

Recruitment Status:

Completed

Sponsor:


Allergan

How clear is this clinincal trial information?

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