RimegepAnt effectIvenesS and tolErability as Migraine Preventive Treatment
NCT06409832 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 100
Last updated 2026-01-21
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.
Conditions
- Migraine
- Migraine With Aura
- Migraine Without Aura
- Chronic Migraine
Interventions
- DRUG
-
Rimegepant 75 mg
Patients using Rimegepant 75 mg orally disintegrating tablet every other day as migraine prevention
Sponsors & Collaborators
-
IRCCS National Neurological Institute "C. Mondino" Foundation
collaborator OTHER -
Società Italiana per lo Studio delle Cefalee
collaborator OTHER -
Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari
collaborator OTHER -
Università degli Studi dell'Aquila
collaborator OTHER -
University of Roma La Sapienza
collaborator OTHER -
Azienda Ospedaliero Universitaria Policlinico Modena
collaborator OTHER -
Ospedale di Piove di Sacco
collaborator UNKNOWN -
Azienda Ospedaliero-Universitaria di Parma
collaborator OTHER -
Azienda Ospedaliera S. Maria della Misericordia
collaborator OTHER -
A.O.U. Città della Salute e della Scienza
collaborator OTHER -
Cliniche Humanitas Gavazzeni
collaborator OTHER -
University of Campania Luigi Vanvitelli
collaborator OTHER -
Ospedale Santo Stefano
collaborator OTHER -
Azienda Policlinico Umberto I
collaborator OTHER -
Auxologico San Luca
collaborator OTHER -
Asst Degli Spedali Civili Di Brescia
collaborator OTHER -
Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta
collaborator OTHER -
University of Florence
lead OTHER
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-03-26
- Primary Completion
- 2027-01-01
- Completion
- 2027-09-30
Countries
- Italy
Study Locations
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