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The relationship between electroencephalogram burst suppression and postoperative delirium in elderly patients under sevoflurane anesthesia:a multicentre, prospective cohort study

The relationship between electroencephalogram burst suppression and postoperative delirium in elderly patients under sevoflurane anesthesia:a multicentre, prospective cohort study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900028171
Enrollment
Unknown
Registered
2019-12-14
Start date
2020-01-01
Completion date
Unknown
Last updated
2020-06-08

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

Conditions

postoperative delirium

Interventions

Case series:sevoflurane anesthesia

Sponsors

Department of Anesthesiology, Huashan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Aged between 65 and 90 years; (2) Patients with gastrointestinal tumors expected for elective surgery under sevoflurane general anesthesia (2h-6h); (3) ASA Physical Status Classification I-III; (4) Agree to participate in the study voluntarily, and sign the written informed consent.

Exclusion criteria

Exclusion criteria: (1) Patients with preoperative history of schizophrenia (including preoperative delirium), and/or taking typical and atypical antipsychotic drugs (Chlorpromazine, Haloperidol, Clozapine, Risperidone, Olanzapine, Quetiapine and extra); (2) Patients with preoperative cognitive dysfunction based on MMSE scale; (3) Severe functional impairment of hearing, vision, and language system; (4) Critically ill (ASA classification IV or above), severe renal dysfunction (requiring of renal replacement therapy), severe hepatic dysfunction (Child-Pugh classification C); (5) Patients planning to enter the ICU after surgery; (6) Identified/suspected of abuse or long-term use of narcotic sedatives or analgesics; (7) Patients with difficult airway that require awake intubation or have been diagnosed with moderate to severe OSAS; (8) Patients with allergies or contraindications to conventional anesthetics; (9) Forehead infections or allergies that not suitable for EEG electrode placement; (10) Patients with a history of general anesthesia within three months; (11) Patients participating in other clinical studies at the same time.

Design outcomes

Primary

MeasureTime frame
Incidence of delirium within the first 5 postoperative days;

Secondary

MeasureTime frame
Length of postoperative hospital stay;Hospital mortality;30-day postoperative mortality;Postoperative complications hypothesized to be associated with anesthetic depth (cardiac arrest, myocardial infarction, stroke, incision infection, etc.);

Countries

??

Contacts

Public ContactYing-wei Wang

Huashan Hospital, Fudan University

wangyingwei@yahoo.com+86 13918690528

Outcome results

None listed

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