About this trial
The goal of this observational study is to evaluate clinical differences in patients who received preventive treatment with medication targeting calcitonin gene-related peptide (CGRP) or its receptor: monoclonal antibodies (erenumab, galcanezumab, fremanezumab, eptinezumab) or gepants (rimegepant, atogepant) during a 2-year period observation phase.
Eligibility criteria
Qualifiers
Migraine diagnosis according to ICHD-III.
Prescription of erenumab, galcanezumab, fremanezumab, eptinezumab, atogepant or rimegepant according to prescriptor criteria and reimbursement criteria according to local regulations.
Signature of informed consent.
Disqualifiers
Presence of headache different from migraine.
Active severe psychiatric condition or cognitive impairment which may affect the ability to consent patient's participation in the study.
Trial design
Treatments tested in this trial
- CGRP antibody or gepant