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Comparison of the Incidence of Delirium Caused by Different Anesthetic Agents in Patients Undergoing Liver Transplantation

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Yonsei University

Status

Enrolling

Conditions

Liver Cirrhosis
Hepatocellular Carcinoma

Study type

Observational

Funder types

Other

Identifiers

NCT06767579
4-2024-1084

Details and patient eligibility

About

This study is a prospective observational study that analyzes the incidence of postoperative delirium in patients undergoing liver transplantation, based on the use of the inhalational anesthetic sevoflurane and the intravenous anesthetic propofol.

Enrollment

350 estimated patients

Sex

All

Ages

19+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adults aged 19 years and older
  • Patients undergoing liver transplantation who are scheduled to receive anesthesia with the inhaled anesthetic sevoflurane or the intravenous anesthetic propofol.

Exclusion criteria

  • Individuals with hearing loss, cognitive impairment or obvious dementia, hepatic encephalopathy, or difficulty in communication.
  • Diagnosed with neurological disorders (e.g., brain hemorrhage, stroke, dementia, Parkinson's disease, cognitive impairment, etc.).

Trial design

350 participants in 2 patient groups

Sevoflurane Inhalation Anesthesia Group
Description:
Sevoflurane Inhalation Anesthesia Group in Liver Transplantation Patients
Propofol Intravenous Anesthesia Group
Description:
Propofol Intravenous Anesthesia Group in Liver Transplantation Patients

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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