RimegepAnt effectIvenesS and tolErability as Migraine Preventive Treatment - Trial NCT06409832
Access comprehensive clinical trial information for NCT06409832 through Pure Global AI's free database. This phase not specified trial is sponsored by University of Florence and is currently Recruiting. The study focuses on Migraine,Migraine With Aura,Migraine Without Aura,Chronic Migraine. Target enrollment is 100 participants.
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Study Focus
Sponsor & Location
University of Florence
Timeline & Enrollment
N/A
Mar 26, 2024
Jan 01, 2026
Primary Outcome
Changes in migraine frequency after three months of treatment,Percentage of 50% Responders (namely patients who presented a reduction of MMDs / = 50% compared to baseline) after three months of treatment with rimegepant
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.
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT06409832
Non-Device Trial