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Analysis of the relationship between EEG burst suppression and poor prognosis in children under general anesthesia and related influencing factors

Analysis of the relationship between EEG burst suppression and poor prognosis in children under general anesthesia and related influencing factors

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200055256
Enrollment
Unknown
Registered
2022-01-05
Start date
2022-01-01
Completion date
Unknown
Last updated
2023-01-23

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

Conditions

burst suppression in children, emergency delirium

Interventions

burst suppression group:Nil
no burst suppression group:Nil

Sponsors

Beijing Children's Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
0.5 Years to 9 Years

Inclusion criteria

Inclusion criteria: 1. American Society of Anesthesiology (ASA) classification I-II; 2. Aged 0.5 to 9 years (the EEG changes in children are most obvious at 0-3 years old, and most delirium in children occurs at 4-9 years old), gender is not limited; 3. The duration of the operation under general anesthesia is more than 30 minutes; 4. Be informed about the purpose and content of this research and sign the consent form.

Exclusion criteria

Exclusion criteria: 1. Subjects with a history of respiratory tract infection within 1 week; 2. Subjects with congenital malformations such as craniocerebral malformations and congenital heart disease; 3. Subjects with a history of craniocerebral injury, possible intracranial hypertension, cerebral aneurysm, cerebrovascular accident, and a history of central nervous system diseases; 4. Subjects with a history of hyperthyroidism; 5. Subjects with any history of neurological or psychiatric disorders; 6. Subjects using sedative or analgesic drugs within 24 hours; 7. Subjects with contraindications to general anesthesia; 8. Subjects with severe liver and kidney dysfunction; 9. Those who are allergic to EEG electrodes or have adverse reactions.

Design outcomes

Primary

MeasureTime frame
burst suppression rate;emergency delirium rate;

Secondary

MeasureTime frame
prolonged awakening time;extended extubation time;

Countries

China

Contacts

Public ContactZhang Jianmin

Beijing Children's Hospital Affiliated to Capital Medical University

zjm428@sina.com+86 13370115019

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 10, 2026