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A study on the correlation between residual hepatic perfusion indexes planned before hepatic cancer resection and postoperative liver function

A study on the correlation between residual hepatic perfusion indexes planned before hepatic cancer resection and postoperative liver function

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400080252
Enrollment
Unknown
Registered
2024-01-24
Start date
2024-02-01
Completion date
Unknown
Last updated
2024-01-28

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

Conditions

hepatocellular carcinoma (HCC)

Interventions

High HAC group/Low HAC group:None

Sponsors

The Second Affiliated Hospital of Kunming Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Clinical diagnosis of HCC according to the NHLBI Guidelines for the Diagnosis and Treatment of Primary Liver Cancer (2022 edition), or diagnosis of HCC by liver puncture biopsy or postoperative pathology, and preoperative hepatocellular carcinoma BCLC stage 0-A; (2) Preoperative liver function Child-pugh classification is grade A or B, with no obvious contraindication to surgery; (3) Received radical hepatectomy treatment; (4) Not having received systemic treatments such as hepatic artery chemoembolization, hepatic artery embolization, hepatic artery perfusion chemotherapy, local treatment with percutaneous anhydrous ethanol injection therapy, or targeted immunization before surgery; (5) Triple-phase CT scan within 2 weeks prior to surgery.

Exclusion criteria

Exclusion criteria: (1) Patients with complete occlusion of the main portal vein trunk, or with arteriovenous leakage; (2) Cases if the peak aortic enhancement is not in the arterial phase or the peak portal vein enhancement is not in the venous phase; (3) Patients with R1/R2 resection, surgery for recurrent HCC, or malignant tumors of other organs during the same period; (4) Patients with other liver diseases (e.g., Buga syndrome) and heart, brain, and kidney diseases; (5) Patients with combined HIV infection; (6) Patients with incomplete clinical information.

Design outcomes

Primary

MeasureTime frame
Hepatic artery coefficient;Portal vein coefficient;total bilirubin;INR;albumin;ProthrombinTime;

Countries

China

Contacts

Public ContactKe Yang

The Second Affiliated Hospital of Kunming Medical University

keyang1218@126.com+86 158 0887 5159

Outcome results

None listed

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