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

This study will assess the safety and efficacy of botulinum toxin Type A for the treatment of urinary incontinence overactive bladder in patients with a spinal cord injury or multiple sclerosis.

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Full Description

Botulinum toxin Type A 300U has been discontinued from the study after regulatory approval of botulinum toxin Type A 200U. Patients remaining in the study who were allocated to receive botulinum toxin Type A 300U at treatment 2 (and had not yet received it) will receive botulinum toxin Type A 200U instead.

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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.
Neurological respiratory impairment and abnormal pulmonary function test results

Exclusion Criteria:

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

Study is for people with:

Multiple Sclerosis

Phase:

Phase 3

Estimated Enrollment:

41

Study ID:

NCT00439140

Recruitment Status:

Terminated

Sponsor:

Allergan

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There is 1 Location for this study

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Philadelphia Pennsylvania, , United States

Herston Queensland, , Australia

Victoria British Columbia, , Canada

Chennai , , India

How clear is this clinincal trial information?

Study is for people with:

Multiple Sclerosis

Phase:

Phase 3

Estimated Enrollment:

41

Study ID:

NCT00439140

Recruitment Status:

Terminated

Sponsor:


Allergan

How clear is this clinincal trial information?

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