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Qualification of EEG obtained from EEG interface device during general anesthesia

Qualification of EEG obtained from EEG interface device during general anesthesia - Exploring a low-cost EEG monitor

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000014890
Enrollment
30
Registered
2014-08-20
Start date
2014-08-20
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

patients who were scheduled surgery under general anesthesia

Interventions

None listed

Sponsors

Osaka University Graduate School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with ASA-PS I or II who were obtained written informed consent

Exclusion criteria

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.

Design outcomes

Primary

MeasureTime frame
test the robustness of EEGs obtained from the devices against the electric noise during general anesthesia

Countries

Japan

Contacts

Public ContactSatoshi Hagihira

Osaka University Graduate School of Medicine Department of Anesthesiology and Intensive Care Medicine

hagihira@anes.med.osaka-u.ac.jp06(6879)3133

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026