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Application of EEG Monitoring and Artificial Intelligence Analysis Technology in Establishing Predictive Models of Anesthesia Depth and noxious stimuli in Children

Application of EEG Monitoring and Artificial Intelligence Analysis Technology in Establishing Predictive Models of Anesthesia Depth and noxious stimuli in Children

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500109260
Enrollment
Unknown
Registered
2025-09-16
Start date
2025-09-16
Completion date
Unknown
Last updated
2025-09-22

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

Conditions

Anesthesia depth and noxious stimuli

Interventions

Sevoflurane observation group:None
Propofol Observation group:None

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 18 Years

Inclusion criteria

Inclusion criteria: 1.Age: 6 months to 18 years (inclusive but exclusive), undergoing elective non-cardiac surgery under general anesthesia; 2.ASA I-III grade; 3. The expected anesthesia time (defined as the period from anesthesia induction to the discontinuation of the anesthetic drug) is greater than 30 minutes; 4. Obtain permission from parents or guardians (sign an informed consent form).

Exclusion criteria

Exclusion criteria: 1. Born with congenital malformations or other diseases that may affect brain development (such as neonatal hypoxic-ischemic encephalopathy, genetic diseases, chromosomal diseases, etc.); 2. Suffering from neurological, mental disorders or severe cardiovascular system diseases (such as complex congenital heart disease, cyanotic congenital heart disease); 3. The area for electroencephalogram (EEG) monitoring conflicts with the area for surgical disinfection. 4. Long-term treatment with sedatives (such as propofol, midazolam, dexmedetomidine, ketamine, etc.), opioids (such as morphine, fentanyl, etc.) or antipsychotic drugs; 5. Known to be allergic to or have adverse reactions to electroencephalogram or electrocardiogram electrode adhesives; 6. Children who are not suitable for inhalation anesthesia (such as those with a family history of malignant high fever or those requiring intraoperative neurological function monitoring, etc.). 7. Allergic to drugs, sensors, etc. used in the research.

Design outcomes

Primary

MeasureTime frame
Predictive models of anesthesia depth for children;

Secondary

MeasureTime frame
EEG features of noxious stimuli;Incidence of postoperative delirium in children and related EEG features;

Countries

China

Contacts

Public ContactYuyi Zhao

West China Hospital, Sichuan University

zhaoyuyi@wchscu.cn+86 189 8060 6837

Outcome results

None listed

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