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Occipital Transcutaneous Stimulation in Chronic Migraine

Transcutaneous Suboccipital Neurostimulation for the Treatment of Chronic Migraine

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02307071
Acronym
OSCRO
Enrollment
20
Registered
2014-12-03
Start date
2014-11-30
Completion date
2015-12-31
Last updated
2015-05-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Migraine

Brief 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.

Interventions

DEVICECefaly Kit Arnold

Occipital 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.

Sponsors

University of Liege
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* diagnosis of chronic migraine (ICHD III beta 1.3) with or without medication overuse

Exclusion criteria

* other diseases

Design outcomes

Primary

MeasureTime frame
Monthly frequency of migraine days2 months treatment

Secondary

MeasureTime frame
Monthly frequency of headache days2 months
Monthly frequency of total headache days2 months
Cumulative monthly headache hours2 months
Monthly acute drug intake2 months

Countries

Belgium

Contacts

Primary ContactAnna Cosseddu, MD
cossedduanna@gmail.com+3242256925

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026