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The Efficacy and Safety of tDCS in Patients With Mild Dementia

Mild Dementia Clinical Trial

Official title:
In a Patient With Mild Dementia, Improvement of Cognitive Function Using YMS-201B, To Evaluate the Effectiveness and Safety, Randomized, Double-blinded, Sham Control Comparison, Confirmatory

Clinical Trial Summary

This study evaluated the effectiveness and safety of improving Mild Dementia by applying tDCS for 26 weeks to patients with Mild Dementia.

Clinical Trial Description

Patients received tDCS for 30 minutes with an intensity of 1.5 to 2 mA. tDCS was applied over the left (anode) and right (cathode) dorsolateral prefrontal cortex (DLPFC) 5~7 times a week and they were evaluated every 26weeks through questionnaires. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05495113
Study type Interventional
Source Ybrain Inc.
Contact Kiwon Lee, PhD
Phone +82-10-3911-3010
Email kwanghyuk.lee@ybrain.com
Status Recruiting
Phase N/A
Start date December 1, 2019
Completion date December 30, 2022
View Details
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