Migraine Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You have been diagnosed with chronic migraine (frequent migraines occurring most days of the month)
- You have been diagnosed with episodic migraine, either with or without warning symptoms (such as visual disturbances) before the headache
- You have already tried 3 or more standard migraine prevention medications that did not work well enough for you
- Your health insurance covers the cost of the medication used in this trial
- If you are joining as a healthy volunteer (not a migraine patient), you must have no diagnosed long-term illness and no current infection that requires medication
Who may not be able to join:
- You are currently pregnant or breastfeeding
- You have had brain or nervous system surgery in the last 12 months
- You have had heart bypass surgery or a procedure to restore blood flow to the heart in the last 12 months
- You have a history of mini-strokes (TIA), stroke, chest pain conditions (angina), heart attack, or poorly controlled high blood pressure
- You have a known allergy or sensitivity to a type of migraine treatment called anti-CGRP antibodies
- You have a condition (other than migraine) that could affect the results of tests measuring your body's automatic functions, such as heart rate or blood pressure responses (confirm with trial site)
- If you are joining as a healthy volunteer, neither you nor any close family member has a history of migraine
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Christian Wöber, Prof. MD, Medical University of Vienna
Phone: +43 (0)1 40400 - 31170
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Change from Day 0 Cardiovagal Autonomic Dysfunction (CAD) at 5 months; Change from Days 1-31 Cardiovagal Autonomic Dysfunction (CAD) at 5 months; Change from Days 0 Cardiovagal Autonomic Dysfunction (CAD) at Days 1-31
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.