The purpose of this non interventional research is to set up a French database, initially for 3 years, of patients suffering from refractory chronic headache disorders (chronic migraine, cluster headache, chronic paroxysmal hemicranias, SUNCT syndrome, hemicrania continua, cervicogenic headache disorders), and treated by occipital nerves stimulation. Every team using this neuromodulation approach in France is likely to participate in the network. Fifty patients a year are expected. They will be informed about data which are collected and why they are collected. The data will come from medical files and questionnaires filling out by the patients. The data will be collected on a case report form adapted to each refractory chronic headache disorder. The case report form pages will be faxed to the coordinating team who will enter the data in the database and analyse the data in a descriptive manner. These data are social and demographic data, medical data (headache features, headache functional and emotional impact, medications, and concomitant medical conditions), technical data (kind of electrodes and implantable pulse generator used, stimulation parameters chosen), and safety data. This research should provide an update on practices, an evaluation of the efficacy and long term safety of occipital nerves stimulation, and perhaps help in identifying response predictive factors to this neuromodulation approach.
Study Type
OBSERVATIONAL
Enrollment
246
Hopitaux Civil de Colmar
Colmar, Haut-rhin, France
Clermont Ferrand CHU
Clermont-Ferrand, France
Annecy Genevois CHU
Épagny, France
Grenoble CHU
Grenoble, France
Lille CHU
Lille, France
Limoges CHU
Limoges, France
HCL
Lyon, France
APHM
Marseille, France
Nancy CHU
Nancy, France
Nantes CHU
Nantes, France
...and 6 more locations
observation of a disease or medical condition under normal conditions
social and demographic data, medical data (headache features, headache functional and emotional impact, medications, and concomitant medical conditions), technical data (kind of electrodes and implantable pulse generator used, stimulation parameters chosen), and safety data.
Time frame: at each visit (up to 4 years)
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