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A prospective study of EEG-based desflurane anesthesia and postoperative delirium

A prospective study of EEG-based desflurane anesthesia and postoperative delirium - A prospective study of EEG-based desflurane anesthesia and postoperative delirium

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000044419
Enrollment
50
Registered
2021-06-03
Start date
2021-07-01
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

Not specified

Interventions

None listed

Sponsors

Tohoku University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The eligibility criteria are patients who meet the following conditions. (1) Patients scheduled for abdominal surgery of 120 minutes or more at Tohoku University Hospital (2) Patients who require general anesthesia or general anesthesia with epidural anesthesia (3) Adult patients aged 20 years or older (4) Gender is not required.

Exclusion criteria

Exclusion criteria: (1) Patients with central nervous system disorders and psychiatric disorders (2) Patients who regularly use CNS-acting drugs (3) Patients who drink a lot of alcohol or use illegal drugs (4) Patients with a history or family history of malignant hyperthermia (5) Patients who cannot communicate in Japanese (6) Patients who had an adverse reaction to desflurane and required a change in anesthetic (7) Patients who could not be awakened and extubated in the operating room immediately after the completion of surgery

Design outcomes

Primary

MeasureTime frame
Correlation with desflurane concentration, depth of anesthesia, and age

Secondary

MeasureTime frame
Calculation of optimal desflurane concentration for each age group

Countries

Japan

Contacts

Public ContactKOTOE KAMATA

Tohoku University School of Medicine Department of Anesthesiology and Perioperative Medicine

kotoe.kamata.c3@tohoku.ac.jp+81-22-717-7321

Outcome results

None listed

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