Change in characteristics of stereoelectroencephalography induced by propofol-based anesthesia in children

Status

Recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2300071918

Enrollment

Unknown

Registered

2023-05-29

Start date

2022-11-01

Completion date

Unknown

Last updated

2023-06-12

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

Conditions

propofol-induced consciousness change

Interventions

Case series:N/A

Eligibility

Sex/Gender

All

Age

1 Years to 16 Years

Inclusion criteria

Inclusion criteria: 1.epileptic patients scheduled for placement of intracranial stereoelectrodes ; 2.children aged 1-16 years who can have simple communication with investigators; 3.planning to implant intracranial stereoelectrodes in epileptic foci located in frontal or temporal lobe; 4.informed consent was signed by parents of participants.

Exclusion criteria

Exclusion criteria: 1.not planning to place intracranial stereoelectrodes in frontal lobe; 2.allergic to propofol or beans; 3.already participated in other clinical trials; 4.not suitabe for inclusion judged by investigators; 5.refusal to sign informed consent.

Design outcomes

Primary

Measure	Time frame
Permutation cross mutual information(PCMI);	—

Secondary

Measure	Time frame
permutation entropy;	—

Countries

China

Contacts

Public ContactLi-Xin Cai

Peking University First Hospital

songlinlinlynkia@163.com+86 135 0130 9217

Outcome results

None listed

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