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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 8 June 2015
Main ID:  NCT02307071
Date of registration: 01/12/2014
Prospective Registration: No
Primary sponsor: University Hospital of Liege
Public title: Occipital Transcutaneous Stimulation in Chronic Migraine OSCRO
Scientific title: Transcutaneous Suboccipital Neurostimulation for the Treatment of Chronic Migraine
Date of first enrolment: November 2014
Target sample size: 20
Recruitment status: Recruiting
URL:  http://clinicaltrials.gov/show/NCT02307071
Study type:  Interventional
Study design:  Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment  
Phase:  Phase 4
Countries of recruitment
Belgium
Contacts
Name:     Anna Cosseddu, MD
Address: 
Telephone: +3242256925
Email: cossedduanna@gmail.com
Affiliation: 
Name:     Anna Cosseddu, MD
Address: 
Telephone: +3242256925
Email: cossedduanna@gmail.com
Affiliation: 
Name:     Delphine Magis, MD, PhD
Address: 
Telephone:
Email:
Affiliation:  University of Liège
Name:     Jean Schoenen, MD, PhD
Address: 
Telephone:
Email:
Affiliation:  University of Liège
Key inclusion & exclusion criteria

Inclusion Criteria:

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

Exclusion Criteria:

- other diseases



Age minimum: 18 Years
Age maximum: 65 Years
Gender: Both
Health Condition(s) or Problem(s) studied
Chronic Migraine
Intervention(s)
Device: Cefaly Kit Arnold
Primary Outcome(s)
Monthly frequency of migraine days [Time Frame: 2 months treatment]
Secondary Outcome(s)
Monthly frequency of total headache days [Time Frame: 2 months]
Cumulative monthly headache hours [Time Frame: 2 months]
Monthly acute drug intake [Time Frame: 2 months]
Monthly frequency of headache days [Time Frame: 2 months]
Secondary ID(s)
OTSCM
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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