Clinical trial Recruiting at 1 site Phase 4 Interventional Ages 20 to 80

Comparing Propofol and Sevoflurane Anesthesia for Liver Tumor Surgery

Official title: Impact of Propofol-Based Total Intravenous Anesthesia Versus Anesthesia With Sevoflurane

Run by Kaohsiung Medical University Chung-Ho Memorial Hospital · NCT05331911 · Data updated 2026-11-12

This study is testing whether using propofol or sevoflurane for anesthesia during liver tumor surgery helps people with liver cancer recover better and live longer.

More Hepatocellular Carcinoma trials

Quick facts

PhasePhase 4
Study typeInterventional
Ages20 Years to 80 Years
SexAll
Enrollment500 (estimated)
SponsorKaohsiung Medical University Chung-Ho Memorial Hospital
Academic / other
Drugs / interventionschemotherapy, radiation
Locations1 site (Kaohsiung City)
StatusRecruiting
StartedApril 26, 2022
Main results expectedDecember 31, 2026
Study endsMarch 31, 2027
Registry record updatedNovember 30, 2022
Trial IDNCT05331911 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are patients aged 20 to 80 years with ASA class I-III who are scheduled for elective partial hepatectomy due to hepatocellular carcinoma.

Probably not a fit

Patients with severe mental disorders, morbid obesity, or those undergoing emergency surgery will not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial is a two-arm, parallel-group randomized trial that aims to evaluate the long-term outcomes of patients undergoing elective partial hepatectomy for primary liver tumors. Approximately 500 volunteers with hepatocellular carcinoma will be randomly assigned to receive either propofol or sevoflurane for anesthesia maintenance during surgery. The study will monitor various parameters, including overall survival and progression-free survival, as well as postoperative complications and functional capacity. Data will be collected on anesthetic drug dosages, patient demographics, and surgical outcomes to determine the effectiveness of each anesthesia method.

Why it matters

Potential benefit: If successful, this study could provide insights into which anesthesia method leads to better long-term survival outcomes for patients undergoing liver tumor surgery.

How similar studies have gone: Other studies have explored anesthesia methods in surgical settings, but this specific comparison of propofol versus sevoflurane in liver surgery is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Twenty to eighty-year-old.
2. ASA class I-III.
3. Patients undergoing partial hepatectomy for hepatocellular carcinoma under general anesthesia.

Exclusion Criteria:

1. Severe mental disorder
2. Pregnant or lactating women
3. Morbidly obese
4. Allergy to any of the drugs used in this study
5. Recurrent tumor or repeat surgery
6. Biopsy cases
7. Incomplete data collection before the surgery
8. Palliative treatment after surgery
9. simultaneous treatment of other malignancies
10. Combined propofol and inhalation anesthesia or other anesthetics, such as ketamine or dexmedetomidine
11. Diagnosed as benign liver tumor
12. Emergency surgery

Where it's running

  • Kaohsiung Medical University Chung-Ho Memorial Hospital
    Kaohsiung City, Taiwan
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.