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Recruiting NCT05673915

NCT05673915 Study of Transcranial Direct Current Stimulation to Treat Epilepsy

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Clinical Trial Summary
NCT ID NCT05673915
Status Recruiting
Phase —
Sponsor Mayo Clinic
Condition Focal Epilepsy
Study Type INTERVENTIONAL
Enrollment 30 participants
Start Date 2023-04-12
Primary Completion 2026-12

Eligibility & Interventions

Sex All sexes
Min Age 6 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
ActivaDose II 0.1 mA transcranial direct current stimulation (tDCS)ActivaDose II 2.0 mA transcranial direct current stimulation (tDCS)

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 30 participants in total. It began in 2023-04-12 with a primary completion date of 2026-12.

⚠ 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

The purpose of this research is to see to what extent electrical stimulation applied to the scalp (transcranial direct current stimulation or tDCS) can reduce the number and intensity of epileptic seizures.

Eligibility Criteria

Inclusion Criteria * Clinical diagnosis of generalized onset or focal epilepsy or sleep-related epileptic encephalopathy. * Estimated to have at least 2 countable seizures per month or spike-wave index ≥50%. * Has not had control with at least 2 anti-seizure medicines. * Able to maintain a constant medication for duration of the study (rescue meds allowed). * Subject or legally authorized representative is able to understand consent and keep a seizure diary in English. Exclusion Criteria: * A disease likely to progress over course of the study. * Psychogenic non-epileptic seizures. * Suicide attempt or psychiatric hospitalization past 2 years. * A skin condition interfering with scalp electrodes or allergy to silver. * Women will verify not pregnant, and if applicable, have a serum pregnancy test. * Implanted devices (e.g. pacemakers)-except VNS, which is allowed.

Contact & Investigator

Central Contact

Precylla Ruiz

✉ ruiz.precylla@mayo.edu

📞 507-538-6606

Principal Investigator

Brian Lundstrom, MD, PhD

PRINCIPAL INVESTIGATOR

Mayo Clinic

Frequently Asked Questions

Who can join the NCT05673915 clinical trial?

This trial is open to participants of all sexes, aged 6 Years or older, studying Focal Epilepsy. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT05673915 currently recruiting?

Yes, NCT05673915 is actively recruiting participants. Contact the research team at ruiz.precylla@mayo.edu for enrollment information.

Where is the NCT05673915 trial being conducted?

This trial is being conducted at Rochester, United States.

Who is sponsoring the NCT05673915 clinical trial?

NCT05673915 is sponsored by Mayo Clinic. The principal investigator is Brian Lundstrom, MD, PhD at Mayo Clinic. 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: November 2026  ·  Data Methodology