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Recruiting NCT07402954

NCT07402954 Stimulation of External Carotid Artery Circulation

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Clinical Trial Summary
NCT ID NCT07402954
Status Recruiting
Phase
Sponsor The University of Texas Medical Branch, Galveston
Condition Migraine
Study Type INTERVENTIONAL
Enrollment 12 participants
Start Date 2026-01-16
Primary Completion 2027-08

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 100 Years
Study Type INTERVENTIONAL
Interventions
Cadwell Cascade 32 PRO

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 12 participants in total. It began in 2026-01-16 with a primary completion date of 2027-08.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This study is testing a new approach to help people with migraine headaches. Researchers want to find out if using electrical stimulation to affect blood flow in the external carotid artery is safe and practical for helping control headaches. The goal of the study is to determine whether this approach could improve headache symptoms and overall outcomes for people with migraines.

Eligibility Criteria

Inclusion Criteria: * Age ≥18 * Chronic migraine or status migrainosus, or craniofacial pain refractory to maximal medical therapy who are undergoing MMA IA lidocaine infusion. * Subject has provided informed consent. Exclusion Criteria: * Known allergies to lidocaine * Seizure disorder, history of seizures, or increased seizure susceptibility * Intracranial vascular malformations or dural AVF * Hemodynamic instability, any condition where brief hemodynamic shifts may pose risk * Previous MMA intervention or craniotomy that could result in MMA occlusion * Any implanted electronic device (pacemaker, ICD, DBS, VNS, cochlear implant, spinal cord stimulator) * Significant cardiovascular disease (unstable angina, severe arrhythmias, recent MI) * Severe autonomic dysfunction * Active systemic infection * Vulnerable populations (i.e. pregnant individuals, children, prisoners, individuals lacking decision-making capacity, persons with cognitive impairment, those unable to provide informed consent)

Contact & Investigator

Central Contact

Matias Costa, MD

✉ mlcosta@utmb.edu

📞 409-772-0330

Principal Investigator

Peter Kan, MD,MPH

PRINCIPAL INVESTIGATOR

University of Texas Medial Branch

Frequently Asked Questions

Who can join the NCT07402954 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 100 Years, studying Migraine. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07402954 currently recruiting?

Yes, NCT07402954 is actively recruiting participants. Contact the research team at mlcosta@utmb.edu for enrollment information.

Where is the NCT07402954 trial being conducted?

This trial is being conducted at Galveston, United States.

Who is sponsoring the NCT07402954 clinical trial?

NCT07402954 is sponsored by The University of Texas Medical Branch, Galveston. The principal investigator is Peter Kan, MD,MPH at University of Texas Medial Branch. The trial plans to enroll 12 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology