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Recruiting NCT06344338

NCT06344338 Application of tDCS Stimulation in Controlling Refractory Status Epilepticus

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Clinical Trial Summary
NCT ID NCT06344338
Status Recruiting
Phase
Sponsor Xuanwu Hospital, Beijing
Condition Refractory Status Epilepticus
Study Type INTERVENTIONAL
Enrollment 32 participants
Start Date 2024-04-01
Primary Completion 2024-12-31

Eligibility & Interventions

Sex All sexes
Min Age 14 Years
Max Age 80 Years
Study Type INTERVENTIONAL
Interventions
tDCS stimulationTDCS sham-stimulation

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 32 participants in total. It began in 2024-04-01 with a primary completion date of 2024-12-31.

⚠ 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 the study is to assess the efficacy and safety of targeting tDCS stimulation for treatment of Refractory status epilepticus

Eligibility Criteria

Inclusion Criteria: * Age between 14 and 80 year-old with Gender unlimited, * Suitable for EEG monitoring; * Clinical diagnosis of Refractory status epilepticus (status epilepticus that cannot be controlled by two types of antiepileptic drugs and at least one anesthetic); * Informed consent to participate in this study was obtained from the participants or their surrogates Exclusion Criteria: * Unstable vital signs (systolic blood pressure\<90mmHg, heart rate\<60 beats/min, pulse oxygen saturation\<90%); * Having severe skull injury/defect or medical equipment implanted in the head; * Pregnancy; * With any implantable electronic instrument (including pacemakers, vagus nerve stimulators) or metal implanted devices.

Contact & Investigator

Central Contact

research centre of Xuanwu hospital Capital Medical University

✉ liugangqingyi@sina.com

📞 +8601083198899

Principal Investigator

Weibi Chen, Dr

STUDY DIRECTOR

Xuanwu Hospital, Beijing

Frequently Asked Questions

Who can join the NCT06344338 clinical trial?

This trial is open to participants of all sexes, aged 14 Years or older, up to 80 Years, studying Refractory Status Epilepticus. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06344338 currently recruiting?

Yes, NCT06344338 is actively recruiting participants. Contact the research team at liugangqingyi@sina.com for enrollment information.

Where is the NCT06344338 trial being conducted?

This trial is being conducted at Beijing, China.

Who is sponsoring the NCT06344338 clinical trial?

NCT06344338 is sponsored by Xuanwu Hospital, Beijing. The principal investigator is Weibi Chen, Dr at Xuanwu Hospital, Beijing. The trial plans to enroll 32 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