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Recruiting Phase 4 NCT06748209

NCT06748209 Establishing Mobile Transcranial Magnetic Stimulation

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Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT06748209
Status Recruiting
Phase Phase 4
Sponsor Medical University of South Carolina
Condition Treatment Resistant Major Depression
Study Type INTERVENTIONAL
Enrollment 30 participants
Start Date 2025-05-10
Primary Completion 2027-03-01

Eligibility & Interventions

Sex All sexes
Min Age 22 Years
Max Age 80 Years
Study Type INTERVENTIONAL
Interventions
Left prefrontal Transcranial Magnetic Stimulation (TMS)FDA cleared TMS for treating depression

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.

Phase 4 studies follow an already-approved treatment in real-world conditions to monitor long-term safety and effectiveness.

This trial targets 30 participants in total. It began in 2025-05-10 with a primary completion date of 2027-03-01.

⚠ 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

In this pilot study, investigators propose to design and create a portable TMS unit, in a van, and then test out delivering TMS in three different locations in South Carolina, all affiliated with MUSC and within 2-hours driving from Charleston, SC. This study would test out this new delivery mode, and provide valuable feasibility, safety, and efficacy lessons for later refinement and potential widespread adoption of mobile TMS as a treatment option, both in our state and across the US.

Eligibility Criteria

Inclusion Criteria: * Adult (22-80 years old) * Have treatment-resistant depression as defined by the e-Mini, and the antidepressant treatment history form (ATHF short). * Be able to read and communicate in English. * Able to provide their own consent. * Access to a computer with videoconferencing ability for initial consent and telescreen. Exclusion Criteria: * Patients with unstable medical conditions that might make TMS unsafe. This includes current poorly controlled seizures. * Ferromagnetic metal in the head. * Pregnant. * Currently active substance abuse except tobacco.

Contact & Investigator

Central Contact

Mark S George, MD

✉ GEORGEM@MUSC.EDU

📞 8438765142

Principal Investigator

Mark George, MD

PRINCIPAL INVESTIGATOR

Medical University of South Carolina

Frequently Asked Questions

Who can join the NCT06748209 clinical trial?

This trial is open to participants of all sexes, aged 22 Years or older, up to 80 Years, studying Treatment Resistant Major Depression. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

What phase is the NCT06748209 trial and what does that mean for participants?

Phase 4 studies are conducted after a treatment has been approved. They monitor long-term safety and real-world effectiveness in a broader patient population.

Is NCT06748209 currently recruiting?

Yes, NCT06748209 is actively recruiting participants. Contact the research team at GEORGEM@MUSC.EDU for enrollment information.

Where is the NCT06748209 trial being conducted?

This trial is being conducted at Charleston, United States.

Who is sponsoring the NCT06748209 clinical trial?

NCT06748209 is sponsored by Medical University of South Carolina. The principal investigator is Mark George, MD at Medical University of South Carolina. The trial plans to enroll 30 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