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Clinical study on the accuracy of four different domestic anesthesia depth monitors

Clinical study on the accuracy of four different domestic anesthesia depth monitors

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000034839
Enrollment
Unknown
Registered
2020-07-21
Start date
2020-07-27
Completion date
Unknown
Last updated
2020-07-27

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

Conditions

Anesthesia-related complications

Interventions

Gold Standard:Imported BIS monitors.
brands&#32
of&#32
domestic&#32
anesthesia&#32
monitors.

Sponsors

The Second Affiliated Hospital of Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients under general anesthesia who undergo elective abdominal surgery; 2. Aged 18-75 years; 3. ASA grade I-II; 4. Voluntarily participate in this clinical trial and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Those who have a history of neurological or psychiatric diseases or have recently taken drugs that affect the central nervous system; 2. People with hearing and language impairments; 3. Those with severely impaired heart, lung, kidney and liver functions; 4. Weight less than 80% or more than 120% of ideal weight; 5. Participate in other clinical research in the same period; 6. The researchers believe that they have other diseases that are not suitable for participating in this clinical trial.

Design outcomes

Primary

MeasureTime frame
consistency;

Secondary

MeasureTime frame
Correlation;Prediction probability;Incidence;

Countries

China

Contacts

Public ContactHong Li

Department of Anesthesiology, the Second Affiliated Hospital of Army Medical University

lh78553@163.com+86 13608380123

Outcome results

None listed

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