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Recruiting NCT06409832

NCT06409832 RimegepAnt effectIvenesS and tolErability as Migraine Preventive Treatment

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Clinical Trial Summary
NCT ID NCT06409832
Status Recruiting
Phase
Sponsor University of Florence
Condition Migraine
Study Type OBSERVATIONAL
Enrollment 100 participants
Start Date 2024-03-26
Primary Completion 2027-01-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
Rimegepant 75 mg

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 100 participants in total. It began in 2024-03-26 with a primary completion date of 2027-01-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief 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 Criteria

Inclusion Criteria: * 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 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; * 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

Contact & Investigator

Central Contact

Luigi F Iannone, MD

✉ luigifrancesco.iannone@unimore.it

📞 +393896969606

Frequently Asked Questions

Who can join the NCT06409832 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Migraine. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06409832 currently recruiting?

Yes, NCT06409832 is actively recruiting participants. Contact the research team at luigifrancesco.iannone@unimore.it for enrollment information.

Where is the NCT06409832 trial being conducted?

This trial is being conducted at Florence, Italy, Pavia, Italy.

Who is sponsoring the NCT06409832 clinical trial?

NCT06409832 is sponsored by University of Florence. The trial plans to enroll 100 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology