Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-25 @ 12:39 AM
Ignite Modification Date: 2025-12-25 @ 12:39 AM
NCT ID: NCT06221267
Eligibility Criteria: Inclusion Criteria: * Participants with headaches that meet the diagnostic criteria for migraines according to the International Classification of Headache Disorders, 3rd edition (ICHD-3), with or without aura. * Patients prescribed rimegepant by the attending physician for the treatment of migraines. * Signed informed consent form. * Age greater than 18 years. * Not concurrently participating in other interventional clinical studies. Exclusion Criteria: * Patients diagnosed with secondary headaches. * Patients with severe visual, auditory, language, intellectual, memory, consciousness impairments or other conditions that prevent them from completing the questionnaire and follow-up. * Pregnant or lactating female patients. * Patients deemed by the investigator as unsuitable for participation in the study or unable to complete the 4-week follow-up. * Patients with a known history of hypersensitivity reactions to rimegepant or its components. * Evidence in the medical history suggesting the presence of uncontrolled or unstable cardiovascular diseases (such as ischemic heart disease, coronary artery vasospasm, or cerebrovascular ischemia), or a history of myocardial infarction, acute coronary syndrome, percutaneous coronary intervention, cardiac surgery, stroke, or transient ischemic attack within the past 6 months before the screening visit.
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Study: NCT06221267
Study Brief:
Protocol Section: NCT06221267