Migraine Trial, Recruiting NCT07223008 Sponsor: Johns Hopkins University Condition: Migraine
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Migraine Trial, Recruiting

NCT07223008
Recruiting Not Applicable

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:

  • People aged between 18 and 80 years old.
  • People who have been diagnosed with chronic migraine affecting both sides of the head, with their first migraine occurring before age 50, based on recognised international headache diagnostic standards.
  • People whose chronic migraines have not been adequately controlled by, or who could not tolerate, at least 2 different categories of migraine prevention medications (such as beta-blockers, anti-seizure medications, anti-depressants, CGRP antibody treatments, or Botox injections), and whose chronic migraines have continued for at least 12 months before joining, including at least 6 months after those 2 medication categories were tried.
  • People who have not used opioids (such as codeine or morphine) or barbiturates specifically to treat their migraines (use of these medications for other medical reasons is acceptable).
  • People who have had a brain MRI/MRA scan within the past 3 years as part of their routine care, which did not find any other underlying cause for their headaches.
  • People who had at least one day in the past month completely free of migraines, as recorded in a headache diary.
  • People with a MIDAS score of 21 or higher, which reflects severely disabling migraines (confirm with trial site if unsure how to calculate this score).
  • People who are able to read and write in English, as the study assessments have only been validated in English.
  • People who are able to sign their own informed consent form.
  • People who are able to complete all study visits and requirements as outlined in the study plan.

Who may not be able to join:

  • People who have previously had brain or neck vascular surgery or procedures, including brain surgery, shunt placement, certain brain monitoring procedures, or carotid artery surgery.
  • People who have used opioids or barbiturates to treat chronic migraine at any point in the past year.
  • People who currently have a lesion or abnormality in the brain identified on a routine care MRI scan.
  • People who have previously had radiation treatment to the head.
  • People who have been diagnosed with certain other headache types in addition to chronic migraine, such as hemiplegic migraine, basilar migraine, new daily persistent headache, or cluster headache.
  • People with significant liver disease or a creatinine blood level above 2.0 mg/dL indicating reduced kidney function (people with elevated creatinine who are on dialysis may still be considered eligible — confirm with trial site).
  • People with a history of cancer or immune system disorders such as multiple sclerosis, rheumatoid arthritis, or other autoimmune diseases.
  • People with a history of a life-threatening allergic reaction to radiographic contrast dye (people with this allergy may still be considered eligible if the allergy can be managed medically — confirm with trial site).
  • People who are currently enrolled in another migraine study or receiving any experimental migraine treatment.
  • People with additional medical or personal circumstances that the principal investigator determines could interfere with the study results or the person's ability to safely complete the study.
  • People who were previously diagnosed with chronic migraine but whose migraines have since become less frequent due to successful treatment, meaning they now experience episodic rather than chronic 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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 23 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Risheng Xu, MD, PhD, Johns Hopkins School of Medicine

Phone: 000-000-0000

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

Status
Recruiting
Phase
Not Applicable
Registry
ClinicalTrials.gov
Start date
24 April 2026
Est. completion
1 April 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Number of specified adverse events related to the study

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov