Qualification of EEG obtained from EEG interface device during general anesthesia
Not Applicable
- Conditions
- patients who were scheduled surgery under general anesthesia
- Registration Number
- JPRN-UMIN000014890
- Lead Sponsor
- Osaka University Graduate School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Not provided
Exclusion Criteria
(1) patients who had brain disease such as brain tumor, brain infarction, epilepsy etc. (2) patients who recieved drugs before surgery that might have influence on EEG.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method test the robustness of EEGs obtained from the devices against the electric noise during general anesthesia
- Secondary Outcome Measures
Name Time Method
Related Research Topics
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What neural mechanisms does the low-cost EEG interface device monitor during general anesthesia in JPRN-UMIN000014890?
How does the EEG interface device's accuracy compare to standard monitors like BIS in assessing anesthetic depth during surgery?
What EEG biomarkers predict anesthetic depth or recovery in patients using the low-cost interface device in JPRN-UMIN000014890?
Can the EEG interface device detect adverse events like intraoperative awareness or hypoxia in general anesthesia as per JPRN-UMIN000014890?
What alternative EEG monitoring technologies are evaluated for cost-effectiveness in general anesthesia research at Osaka University?