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Anesthesia depth monitoring based on electroencephalogram deep learning

Anesthesia depth monitoring based on electroencephalogram deep learning

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061899
Enrollment
Unknown
Registered
2022-07-09
Start date
2022-08-01
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

anesthesia

Interventions

Group of Sevoflurane:Sevoflurane anesthesia
Group of propofol:Propofol anesthesia

Sponsors

Qilu Hospital of Shandong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 75 years; 2. ASA I-III.; 3. Sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Have participated in other clinical trials within 4 weeks before the start of this study; 2. Drugs that are being taken or have been taken in the 2 weeks prior to the start of this study; 3. Respiratory depression, (lung) airway obstruction or tissue hypoxia; 4. Heart disease (i.e., grade II or above cardiac function); 5. Liver and kidney function is obviously abnormal (the index is more than double the normal value); 6. Nervous system diseases; 7. Allergic to sevoflurane or propofol; 8. Drug and/or alcohol abuse; 9. Pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
Electroencephalogram;End-expiratory concentration of sevoflurane;Target concentration at the effect site of propofol;—

Countries

China

Contacts

Public ContactQi Wu

Qilu Hospital of Shandong University

wuqimed@126.com+86 18560083757

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026