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Clinical Trial Summary

The main objective of this study is to assess the efficacy of the Cefaly® device as an acute treatment of migraine attack in adult patients. The patients will be applied either an active or placebo external neurostimulation for 1 hour during a migraine attack, and will report the pain on a visual analog scale before and after the treatment.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02590939
Study type Interventional
Source Cefaly Technology
Contact
Status Completed
Phase N/A
Start date February 1, 2016
Completion date March 31, 2017

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