RecruitingNCT05903027

Gepant treAtments: EffectIveNess and tolERability (GAINER)

Effectiveness and Tolerability of Rimegepant as Acute Migraine Treatment: a Prospective, Multicentric, Cohort Study (GAINER)

Sponsor

University of Florence

Enrollment

100 participants

Start Date

Jun 15, 2023

Study Type

OBSERVATIONAL

Conditions

Migraine with aura Migraine Chronic Migraine Migraine Without Aura

Summary

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

Eligibility

Min Age: 18 Years

Inclusion Criteria4

Diagnosis of migraine without aura, migraine with aura, or chronic migraine according to the 3rd edition of the International Classification of Headache Disorder (ICHD-III).
At least 3 MMDs
Good compliance to study procedures
Availability of headache diary at least of the preceding months before enrollment

Exclusion Criteria4

Subjects with contraindications for use of gepants;
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.

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Interventions

DRUGRimegepant 75 MG Disintegrating Oral Tablet

Patients using Rimegepant 75 mg orally disintegrating tablet to treat acute migraine attacks

Locations(2)

SOD Centro Cefalee e Farmacologia Clinica, AOU Careggi

Florence, Italy

IRCCS National Neurological Institute "C. Mondino" Foundation

Pavia, Italy

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NCT05903027

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