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RimegepAnt effectIvenesS and tolErability as Migraine Preventive Treatment

Recruitingn/aAges 18 Years - anyAllUniversity of Florence
NCT06409832 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

The purpose of this prospective and multicentric study is to evaluate the effectiveness and tolerability of rimegepant as preventive migraine treatment in a cohort of episodic or chronic migraine patients.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Diagnosis of migraine without aura or migraine with aura, according to the 3rd edition of the International Classification of Headache Disorder (ICHD-III); * At least 4 monthly migraine days; * Good compliance to study procedures; * Availability of headache diary at least of the preceding months before enrollment. Exclusion Criteria: * Subjects with contraindications for use of gepants; * Diagnosis of chronic migraine * Concomitant diagnosis of medical diseases and/or comorbidities that, in the Investigator's opinion might interfere with study assessments; * medical comorbidities that could interfere with study results; * Pregnancy and breastfeeding. * Changes in preventive treatments in the month before the first administration of rimegepant
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What it tests

  • Rimegepant 75 mg
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Where

2 sites
SOD Centro Cefalee e Farmacologia Clinica, AOU Careggi
Florence, Italy
IRCCS National Neurological Institute "C. Mondino" Foundation
Pavia, Italy
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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