A Prospective Real World Study of Rimegepant in the Treatment of Migraine

Status Recruiting

Clinical Trial Summary

The goal of this observational study is to test the effectiveness and safety of Rimegepant in the treatment of migraine patients in real world. The main questions it aims to answer are: - [question 1] the effectiveness and safety of Rimegepant in the acute treatment of migraine - [question 2] the effectiveness and safety of Rimegepant in the long-term treatment of migraine. 1. Participants will be asked to take Rimegepant when they need to treat or prevent a migraine attack. 2. Participants will be asked to record the efficacy data at 0.5, 1, 2, 24, 48h post dose and report any AE to evaluate the effectiveness and safety of Rimegepant in the acute treatment of migraine 3. Participants will be asked to track monthly migraine days and the use of Rimegepant, finish 2 PROs during the follow-ups, report any AE to evaluate the effectiveness and safety of Rimegepant in the long-term treatment of migraine.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05709106
Study type	Observational
Source	Ruijin-Hainan Hospital Shanghai Jiao Tong University School Of Medicine
Contact	Wenyan Kang
Phone	+86 13816512546
Email	kwymed22@163.com
Status	Recruiting
Phase
Start date	February 8, 2023
Completion date	December 30, 2025

View Details

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