Application of tDCS Stimulation in Controlling Refractory Status Epilepticus
Recruiting now · Not applicable · Has a placebo group
Conditions studied: Refractory Status Epilepticus
In brief
The purpose of the study is to assess the efficacy and safety of targeting tDCS stimulation for treatment of Refractory status epilepticus
Key facts
- Study ID
- NCT06344338
- Run by
- Xuanwu Hospital, Beijing
- People needed
- 32
- Starts
- 2024-04-01
- Expected to finish
- 2026-10-01
- Last updated by the study team
- 2026-08-04
Who can join
Age: 14 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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
You may not qualify if…
- 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.
Where it is running
- Xuanwu Hospital, Capital Medical University — Beijing, Beijing Municipality, China (enrolling)
Full record on ClinicalTrials.gov
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