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:
2025-12-24 @ 6:47 PM
Ignite Modification Date:
2025-12-24 @ 6:47 PM
NCT ID:
NCT06532357
Eligibility Criteria:
Inclusion Criteria:
* Patients who used Nurtec and/or triptans as an acute treatment for migraine, with or without a background of preventive treatment (anti-CGRP, Botox or oral migraine preventive medications).
* Male or female participants with migraine
* Having consented to the anonymous use of their data for research
* Currently using Nurtec and/or triptans to treat migraine attacks
Exclusion Criteria:
* Users who did not report using either medication for which they complete the survey within 60 days prior to the survey.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT06532357
Study Brief:
Protocol Section:
NCT06532357