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Clinical Trial Summary

The goal of this clinical trial is to to obtain a significant decrease in seizure frequency in patients with refractory focal epilepsy after applying treatment of cathodal tDCS, compared to sham stimulation drug-resistant epileptic patient. The main questions it aims to answer are: - Changes in quality of life - Percent of newly reported side effects after the stimulation period - Scores in epilepsy severity. Participants will be randomized in a cross-over, and will receive 10 days of tDCS or Sham. Each day will allow 2 periods of 20 minutes stimulation separated by 20 minutes off (with 40 minutes of cathodal stimulation total).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06334952
Study type Interventional
Source Assistance Publique Hopitaux De Marseille
Contact Fabrice Bartolomei, MD, PhD
Phone 0491384990
Email fabrice.bartolomei@ap-hpm.fr
Status Not yet recruiting
Phase N/A
Start date June 1, 2024
Completion date April 30, 2027

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