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Clinical Trial Summary

The purpose of this study is to determine whether 120 Unit, and 240 unit of botulinum toxin A are effective in the treatment of migraine without aura prophylaxis.


Clinical Trial Description

This is a 12-week, prospective double-blinded, randomized, multicenter study of placebo, 120 Unit, and 240 unit of botulinum toxin A ( Dysport ® ) injection for patient with a diagnosis of Migraine without aura according to International Headache Society criteria. It is designed to evaluate the efficacy, safety, tolerability and optimum dose of Botulinum toxin type A (Dysport ®)injection for migraine without aura prophylaxis. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00258609
Study type Interventional
Source Rajavithi Hospital
Contact
Status Completed
Phase Phase 3
Start date February 2003
Completion date June 2004