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UnknownNCT02307071

Occipital Transcutaneous Stimulation in Chronic Migraine

Transcutaneous Suboccipital Neurostimulation for the Treatment of Chronic Migraine

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
20 (estimated)
Sponsor
University of Liege · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

This study evaluates the effect in chronic migraine patients of daily 20 minute-transcutaneous sub occipital neurostimulation using the occipital Cefaly° device.

Detailed description

Chronic migraine is a disabling neurological condition affecting 0.5-2% of the population. CM is difficult to treat and preventive treatment options are limited. Due to the inefficiency of available and the lack of new preventive anti-migraine drug, neurostimulation methods have raised great interest in recent years. The ONSTIM study showed a reduction in headache frequency in 39% of patients treated with active ONS during 12 weeks, compared to no improvement in the "non-effectively" stimulated or medically treated groups.

Conditions

Interventions

TypeNameDescription
DEVICECefaly Kit ArnoldOccipital neurostimulation can have a therapeutic effect in chronic migraine treatment, thus representing a possible therapeutic option in patients that do not respond to any medication.

Timeline

Start date
2014-11-01
Primary completion
2015-09-01
Completion
2015-12-01
First posted
2014-12-03
Last updated
2015-05-28

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT02307071. Inclusion in this directory is not an endorsement.