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OncoMatch/Clinical Trials/NCT05331911

Impact of Propofol-Based Total Intravenous Anesthesia Versus Anesthesia With Sevoflurane on Long-term Outcomes With Patients Undergoing Elective Excision of Primary Liver Tumors

Is NCT05331911 recruiting? Yes, currently enrolling (Jun 2026). This Phase 4 trial studies multiple treatments including Propofol and Sevoflurane for hepatocellular carcinoma.

Phase 4RecruitingKaohsiung Medical University Chung-Ho Memorial HospitalNCT05331911Data as of Jun 2026Location: Taiwan

Treatment: Propofol · SevofluraneThis is a two-arm, parallel-group randomized clinical trial. Routine perioperative care would be performed in volunteers with primary Hepatocellular carcinoma. The study will enroll approximately 500 volunteers to compare the progression-free or overall survival in patients undergoing elective partial hepatectomy for primary liver tumors between propofol and sevoflurane for the maintenance of anesthesia.

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Extracted eligibility criteria

Treatments studied

Other

PropofolSevoflurane

Cancer type

Hepatocellular Carcinoma

Performance status

ASA 1–3

Demographics

Ages 20–80

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT05331911 currently recruiting?

Yes, this trial is currently recruiting patients.

Is there an age limit?

Yes. Patients must be 80 years or younger and at least 20 years old.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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