Interventional study for substances to reduce impedance at the pad/skin interface during electroconvulsive therapy
Not Applicable
- Conditions
- According to the diagnostic criteria for mood (affective) disorders:ICD-10
- Registration Number
- JPRN-UMIN000029134
- Lead Sponsor
- Department of Pychiatry, Kitasato University East hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 10
Inclusion Criteria
Not provided
Exclusion Criteria
Otherwise excluded from study participants. (1) if the person or from the Novotel was discontinued participation in research proposal (2) in the PreTac fluid and Gerad Z-101BA until now or further if any allergic symptoms
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Static impedance (measured with 6 microampere) at placing electrodes on the patient skin and dynamic impedance (measured with 0.9 ampere) during administrating electric current to the brain.
- Secondary Outcome Measures
Name Time Method umber of times spent with saimapad and Postictal Suppression Index (decrease in value immediately after the attack, completed average amplitude of 3 seconds between viewed in percent as reduced the average amplitude of the maximum amplitude of the seizure during 3 seconds, which one of the indicators of the quality of the attack)