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A comparison between bispectral index (BIS) and patient state index (PSI) in elderly patients under general anesthesia with propofol

A comparison between bispectral index (BIS) and patient state index (PSI) in elderly patients under general anesthesia with propofol - A comparison between bispectral index (BIS) and patient state index (PSI) in elderly patients under general anesthesia with propofol

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000040435
Enrollment
50
Registered
2020-05-21
Start date
2020-05-22
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

head, neck and throat disease, extremities and peripheral vessel disease, disease of the chest wall, abdominal wall and perineum

Interventions

The duration of intevention is from obtaining patients&#39
concent and confirming the eligibility criteria to 30th day after the operation. The number of intervention is one.

Sponsors

Yamaguchi University Faculty of Medicine and Health Sciences, Yamaguchi University Hospital, the department of Anesthesiology-Resuscitology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients are included if they meet the following eligibility criteria: (1)65 yr old or older; (2)the expected operative duration is from 2 to 8 hours; (3)scheduled head, neck and throat surgery, extremities and peripheral vessel surgery, the chest wall, abdominal wall and perineum surgery.

Exclusion criteria

Exclusion criteria: Patients are excluded if they meet the following exclusion criteria: (1)cerebral parenchyma disease, cerebrovascular disease, myelopathy, peripheral neuropathy, myopathy, mental disorder, dementia; (2)left ventricular ejection fraction is less than 50%, heart valve disease classified moderate or severe; (3)% vital capacity is less than 80%, and/or forced expiratory volume % in 1 second is less than 70%; (4)liver disease classified Child-Pugh B or C; (5)kidney disease with estimated glomerular filtration rate less than 60 mL/min/1.73m2; (6)diabetes mellitus with HbA1c greater than or equal to 8%; (7)body mass index (BMI) is less than 18.5 or greater than or equal to 25.0; (8)scheduled epidural anesthesia and/or peripheral nerve block; (9)emergency operation.

Design outcomes

Primary

MeasureTime frame
the duration from discontinuation of the propofol to extubation

Secondary

MeasureTime frame
the incidence of awareness with recall during anesthesia, the incidence of postoperative delirium within 7 days after the operation, and the incidence of myocardial infarction and stroke within 30 days after the operation

Countries

Japan

Contacts

Public ContactShuichi Kaneko

Yamaguchi University Faculty of Medicine and Health Sciences, Yamaguchi University Hospital the department of Anesthesiology-Resuscitology

kaneshu@yamaguchi-u.ac.jp0836-22-2291

Outcome results

None listed

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