Postmarketing Clinical Trial of tDCS to Evaluate Cognitive Ability in Depression Patients

Exclusion Criteria

• •1. History of clinically significant medical neurological disease or history of head injury
• •2. In case of mental retardation or cognitive impairment enough to affect the writing of consent form or conducting research
• •3. Severe suicidal risk or psychotic symptoms determined by the clinician
• •4. In the case of a contraindication to the implementation of tDCS (when a metallic auxiliary tool is inserted in the head)
• •5. Those who are judged to have problems with the attachment of EEG and DC stimulation electrodes due to deformities, inflammatory reactions, or other dermatological problems at the electrode attachment site
• •6. Among female subjects who are likely to become pregnant, those who do not agree to contraception by a medically acceptable method for up to 24 weeks after application of the investigational medical device in this clinical trial
• •7. Pregnant women
• •8. Any other person who has reasons to judge that the investigator is unsuitable for participation in the clinical trial