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Evaluation of analgesia by electroencephalogram during general anesthesia

Evaluation of analgesia by electroencephalogram during general anesthesia - Development of EEG based analgesia monitor

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000042843
Enrollment
50
Registered
2020-12-25
Start date
2020-11-06
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

Surgical patients

Interventions

None listed

Sponsors

Kansai Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who satisfied the following all conditions. 1) age is 20 or more and less than 65 2) supine position during surgery 3) ASA-PS is I or II 4) patients who agreed after informed consent

Exclusion criteria

Exclusion criteria: patients who matched either of following conditions. 1) patients who had severe liver dysfunction or severe renal dysfunction 2) pregnant or lactating women 3) patients who had neurological disorder 4) patients who scheduled head or neck surgery 5) patients who are medicated a drug that had interaction with anesthetic or analgesic 6) patients who require legal representative 7) patients who were judged as inappropriate for the current study

Design outcomes

Primary

MeasureTime frame
We administer fentanyl intermittently. We add some amount of fentanyl when peak heights of EEG bicoherence decrease below previously defined threshold, and compare them with those 5 minutes after fentanyl administration.

Countries

Japan

Contacts

Public ContactSatoshi Hagihira

Kansai Medical University Department of Anesthesiology

hagihirs@hirakata.kmu.a.cjp072-804-2683

Outcome results

None listed

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