EMBRACE-OBS: Single-Site Observational Registry of Patient-Reported Outcomes Following MMA Embolization for Migraine
Part of paid clinical trials in Tacoma, Washington.
- Sponsor
- Cortex Neurovascular
- Study ID
- NCT07652034
- Status
- Not Yet Recruiting
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Conditions
- Chronic Migraine Headache
- Migraine
- Migraine Disorders
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 64 Years
- Healthy Volunteers
- Not accepted
Interventions
- Middle Meningeal Artery Embolization — PROCEDUREMiddle meningeal artery (MMA) embolization performed as part of routine clinical care at the discretion of the treating physician. The procedure is independent of study participation and is not assigned by the study protocol. The research activity consists solely of accessing and analyzing data already documented through routine clinical care.
Study Details
EMBRACE-OBS is the first phase of the EMBRACE research program. This single-site observational registry accesses and analyzes patient-reported outcome data already collected through routine clinical care from adults with migraine who have undergone or plan to undergo middle meningeal artery (MMA) embolization. The study describes changes in headache frequency, headache severity, medication use, migraine-related disability, quality of life, and reported adverse events over time without influencing clinical care.
Key Dates
- Start date
- Jul 1, 2026
- Status verified
- Jun 2026
- Primary completion
- Jun 1, 2028
- Completion
- Jun 1, 2028
Study Design
- Enrollment
- 50 participants (estimated)
Arms
- Arm: Migraine Patients Undergoing MMA EmbolizationAdults aged 18 to 64 years with a diagnosis of migraine who have undergone or plan to undergo middle meningeal artery (MMA) embolization as part of routine clinical care. Participants are enrolled in an observational registry that accesses and analyzes clinical and patient-reported outcome data already documented through routine care. Study participation does not influence clinical management, procedural technique, device selection, or follow-up.
Primary Outcome Measure
Change in Patient-Reported Headache Frequency [ Time Frame: Baseline and 12 Months ]
Central Contacts
- Dennis Wang, Principal Investigator, MD253-284-0841
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Cortex Neurovascular / TRA Union | Tacoma | Washington | 98405 | Dennis O Wang, MD (PRINCIPAL_INVESTIGATOR) |
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