Neurosurgical craniotomy patient occipital SEDline monitoring with frontal region Monitoring effect consistency studies

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2400082815

Enrollment

Unknown

Registered

2024-04-09

Start date

2023-11-05

Completion date

Unknown

Last updated

2025-01-13

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

Conditions

Intracranial tumors

Interventions

Trail group:NA

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Age 18~65 years old (2) ASA I.-III. (3) Neurosurgical Craniotomy patients (4) Fill in the informed consent form and voluntarily participate in this study

Exclusion criteria

Exclusion criteria: (1) Preoperative EEG abnormality or preoperative delirium, coma (2) Broken skin or infection at the electrode placement site (3) Central nervous system diseases such as Parkinson's and epilepsy (4) Severe alcohol and drug abuse (5) Antidepressant and antiepileptic drug application (6) Patients with cerebral infarction and TIA seizures in the past three months (7) Patients with neurological diseases such as stroke and traumatic brain injury (8) Those with pacemakers installed

Design outcomes

Primary

Measure	Time frame
Frontal and occipital PSI consistency and difference;	—

Secondary

Measure	Time frame
Frontal and occipital SEFL,SEFR,ARTF,EMG,SR consistency;	—

Countries

China

Contacts

Public ContactWang Tianlong

shou du yi ke da xue xuan wu yi yuan ma zui ke

w-tl5595@hotmail.com+86 138 1110 9032

Outcome results

None listed

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