RecruitingNCT06409832

RimegepAnt effectIvenesS and tolErability as Migraine Preventive Treatment

RimegepAnt effectIvenesS and tolErability as Migraine Preventive Treatment: a Prospective, Multicentric, Cohort Study (RAISE)


Sponsor

University of Florence

Enrollment

100 participants

Start Date

Mar 26, 2024

Study Type

OBSERVATIONAL

Conditions

Summary

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.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Rimegepant 75 mg for people with chronic migraine, migraine, and other related conditions. The study is currently recruiting participants at 2 locations. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGRimegepant 75 mg

Patients using Rimegepant 75 mg orally disintegrating tablet every other day as migraine prevention


Locations(2)

SOD Centro Cefalee e Farmacologia Clinica, AOU Careggi

Florence, Florence, Italy

IRCCS National Neurological Institute "C. Mondino" Foundation

Pavia, Pavia, Italy

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NCT06409832


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