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RecruitingNCT07402954

Safety and feasibility of artery stimulation for treatment-resistant migraine

About this titleRead the official source — NCT07402954
Device studyAges 18–100United StatesBipolarity
The study in practice

Understand this study

Who could participate?

Listed age limits: 18 years to 100 years.

What will I do during this study?

Adults with chronic migraine, status migrainosus, or certain persistent facial pain who are already scheduled for an intra-arterial lidocaine infusion may be eligible for this Galveston study. Before the planned infusion, clinicians apply electrical pulses through the external carotid circulation and monitor vital signs, neurological status, and headache severity. The study is evaluating this procedure; it has not established that it improves headaches. Other eligibility criteria apply.

Listed locations
GalvestonSee all locations and recruitment

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What to know before participating

A point to clarify

This summary does not cover all risks or eligibility requirements. What risks or changes to my care would apply to me?

Study clarity

Things to check before joining

Study start dateStarted: January 16, 2026
Recruitment status
Recruiting
Enrollment listed in the registry
12
Sponsor
The University of Texas Medical Branch, Galveston
Sponsor type
University
Study type
Device
Intervention type
DEVICE
Study phase
Not clearly listed
Locations
United States
Age range
From 18 Years to 100 Years
Official registry ID
NCT07402954
Official title
Show the full official title

Feasibility and Safety of Endovascular Bipolar Stimulation of the Middle Meningeal Artery for Refractory Headaches (MMA-Stim)

Recruitment & locations

Currently recruiting

Galveston

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FAQ

Questions about this study

Who is behind this study?

The study sponsor is The University of Texas Medical Branch, Galveston, a university.

Who can participate?

Listed age limits: 18 years to 100 years.

Is this study still recruiting?

The registry lists this study as recruiting.

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