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Clinical Trial Summary

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


Clinical Trial Description

After being informed about the study and potential risks, the recruited patients, giving written informed consent, will be determined of the eligibility for study entry. The patients who meet the eligibility requirements will be randomized in a 1:1 ratio to undergo targeting tDCS stimulation (up to 10 times) or sham stimulation. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06344338
Study type Interventional
Source Xuanwu Hospital, Beijing
Contact research centre of Xuanwu hospital Capital Medical University
Phone +8601083198899
Email liugangqingyi@sina.com
Status Recruiting
Phase N/A
Start date March 31, 2024
Completion date March 31, 2025

See also
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Completed NCT04333082 - Refractory Status Epilepticus Treatment: Quality and Efficacy of Coma Induction