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NCT06409832Recruiting

RimegepAnt effectIvenesS and tolErability as Migraine Preventive Treatment

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

Source: ClinicalTrials.gov · Last updated 11 Jun 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Observational
Enrollment
100 (estimated)
First submitted
5 Apr 2024
Start date
26 Mar 2024
Primary completion date
1 Jan 2027
Lead sponsor
University of Florence
Diseases
Migraine
NCT number
NCT06409832

What you commit to

  • Study type: Observational
  • Planned participants: 100
  • From 26 Mar 2024 to the primary completion date, 1 Jan 2027
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Concomitant diagnosis of medical diseases and/or comorbidities that, in the Investigator's opinion might interfere with study assessments;
  • Changes in preventive treatments in the month before the first administration of rimegepant

Other

  • Subjects with contraindications for use of gepants;
  • Diagnosis of chronic migraine
  • medical comorbidities that could interfere with study results;
  • Pregnancy and breastfeeding.

Who the study is looking for

  • 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.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
SOD Centro Cefalee e Farmacologia Clinica, AOU Careggi
Coordinator of this site? Confirm its status
FlorenceItalyRecruiting
IRCCS National Neurological Institute "C. Mondino" Foundation
Coordinator of this site? Confirm its status
PaviaItalyRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.