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Clinical Trials/NCT06767579
NCT06767579
Recruiting
Not Applicable

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

Yonsei University1 site in 1 country350 target enrollmentOctober 24, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hepatocellular Carcinoma
Sponsor
Yonsei University
Enrollment
350
Locations
1
Primary Endpoint
incidence of postoperative delirium
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
October 24, 2024
End Date
October 17, 2028
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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.).

Outcomes

Primary Outcomes

incidence of postoperative delirium

Time Frame: from postoperative day 0 to postoperative day 7

At least two times a day during the hospitalization period. Patients diagnosed with delirium using the CAM were evaluated for the duration, symptoms, and type of delirium (e.g., reduced awareness of the environment; poor cognitive skills; behavioral changes; and emotional disturbances). \*\* Confusion assessment methods(CAM) diagnostic algorism (positive or negative result, positive means delirium) CAM is considered positive if features 1 and 2 are present, with at least one of features 3 or 4. Below are the four criteria of features : 1. Acute onset and fluctuating course Determined by collateral history or repeated clinic assessment 2. Inattention Counting from 20-1 is a simple (if blunt) test for this 3. Disorganized thinking 4. Altered levels of consciousness

Secondary Outcomes

  • comprehensive geriatric assessment(CGA)(Participants will be followed for the duration of their hospital stay and until their visit within one month after discharge, with an expected average of 4 weeks)
  • duration of delirium(Participants will be followed for the duration of their hospital stay and until their visit within one month after discharge, with an expected average of 4 weeks)
  • total score of QOR-40(Participants will be followed for the duration of their hospital stay and until their visit within one month after discharge, with an expected average of 4 weeks)
  • type of delirium(Participants will be followed for the duration of their hospital stay and until their visit within one month after discharge, with an expected average of 4 weeks)

Study Sites (1)

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