Multiple Sclerosis Clinical Trial
A Long-term Follow-up Study of Botulinum Toxin Type A in Patients With Overactive Bladder as a Result of Spinal Injury or Multiple Sclerosis
Summary
The purpose of this study is to assess the long-term safety and effectiveness of botulinum toxin type A on patients with overactive bladder as a result of spinal cord injury or multiple sclerosis. This is a follow-up study to two Allergan sponsored studies (NCT00311376 and NCT00461292).
Full Description
Botulinum toxin Type A 300U has been discontinued from the study. Patients remaining in the arm containing botulinum toxin Type A 300U will receive botulinum toxin Type A 200U moving forward. Also, the masking of the study is now open-label.
Eligibility Criteria
Inclusion Criteria:
Patient has participated in study 191622-515 or 191622-516 and the following criteria fulfilled:
Patient completed at least 52 weeks in the preceding study.
No longer than 6 months has elapsed since completion of the preceding study
Patient has not received any prohibited medications during any intervening period between the preceding study and this long-term study.
Exclusion Criteria:
History or evidence of pelvic or urologic abnormality.
Previous or current diagnosis of bladder or prostate cancer.
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There is 1 Location for this study
Middlebury Connecticut, , United States
Randwick , , Australia
Innsbruck , , Austria
Ghent , , Belgium
Rio de Janeiro , , Brazil
Victoria British Columbia, , Canada
Ostrava , , Czechia
Salouel , , France
Kiel , , Germany
Florence , , Italy
Amsterdam , , Netherlands
Epsom , , New Zealand
Poznan , , Poland
Porto , , Portugal
Moscow , , Russian Federation
Singapore , , Singapore
Presov , , Slovakia
Pretoria , , South Africa
Tenerife , , Spain
Hualien , , Taiwan
Kiev , , Ukraine
London , , United Kingdom
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