MMA Embolization for Refractory Chronic Migraine
Cerenovus, Part of DePuy Synthes Products, Inc. · NCT06735833
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–65 · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Not applicable
- Target enrollment
- 70
- US sites recruiting
- 8
- Study start
- April 23, 2025
- Record last updated
- September 25, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
This is a prospective, multi-center, feasibility study to investigate safety and effectiveness of TRUFILL n-BCA liquid embolic system in bilateral middle meningeal artery (MMA) embolization for the treatment of refractory chronic migraine.
Being studied: Middle Meningeal Artery embolization
Conditions: Migraine Disorders
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Participant Inclusion Criteria, Candidates for this study must meet ALL the following inclusion criteria:
- Patient is between 18 and 65 years of age (inclusive) at the time of consent
- Age of onset of Chronic Migraine \<= 64 years
- Age of onset of migraine diagnosis \< 50 years
- Patient has a current diagnosis of refractory migraine
- Patient has a current diagnosis of Chronic migraine
Participant Exclusion Criteria, Candidates will be excluded from participation if ANY of the following apply:
- Patients with a history for the last 2 years of other primary headache types, or secondary headache types except medication overuse headache
- Patients with diagnosis of hemiplegic migraine or migrainous infarct
- Patients with current regular use of Opioids, Cannabis, Medical Marijuana, etc
- Women who are pregnant, lactating, or who are of childbearing age
- Current involvement in an investigational (drug, device, etc.) clinical trial that may confound study endpoints. Participants in observational, natural history, and/or epidemiological studies not involving intervention are eligible. Sponsor approval is required
Recruiting US locations
John Muir Physician Network Clin. Research Center
Walnut Creek, CA 94598
Hartford Hospital
Hartford, CT 06032
University of Buffalo Medical Center
Buffalo, NY 14203
Mount Sinai
New York, NY 10029
Stony Brook University Medical Center
Stony Brook, NY 11794
Thomas Jefferson University Hospital
Philadelphia, PA 19107
Semmes Murphey Foundation
Memphis, TN 38120
West Virginia University
Morgantown, WV 26506
Study contacts (from the official record)
- Study Contact · RA-MIGRAINECNV202302@ITS.JNJ.com
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