Clinical Trials Directory

Trials / Completed

CompletedNCT06245785

Liver Resection for Patients With Hepatocellular Carcinoma and Impaired Liver Function

Liver Resection for Patients With Hepatocellular Carcinoma and Impaired Liver Function: A Chinese Multicenter Observational Study

Status
Completed
Phase
Study type
Observational
Enrollment
2,200 (actual)
Sponsor
Tang-Du Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers

Summary

Hepatic dysfunction limits the therapeutic options for hepatocellular carcinoma (HCC), which is closely associated with patient prognosis. Established practice guidelines for patients with HCC and impaired liver function are lacking. The treatment allocation in these populations is heterogeneous and remains controversial. This study compared the survival benefits of liver resection (LR) and transarterial chemoembolisation (TACE) in patients with HCC and impaired liver function.

Conditions

Interventions

TypeNameDescription
PROCEDUREtransarterial chemoembolisationBefore TACE, hepatic arteriography was performed to evaluate the vascular anatomy and tumour vascularity. During TACE, a vascular catheter was selectively inserted into the tumour-feeding artery with an injection containing a mixture of doxorubicin (10-50 mg) and lipiodol (2-20 mL), followed by embolisation using gelatin sponge particles. TACE was repeated when residual viable tumours were confirmed or new lesions developed in patients with adequate liver function. Laboratory assessments were performed every four to six weeks. Radiological evaluation using contrast-enhanced computed tomography (CT) or magnetic resonance imaging (MRI) was recommended during weeks 4 and 8 after treatment and every 8 weeks thereafter. However, in clinical practice, the intensity of follow-up depends on an individual's baseline characteristics and response to the last treatment.

Timeline

Start date
2023-01-01
Primary completion
2023-04-01
Completion
2023-12-01
First posted
2024-02-07
Last updated
2024-02-07

Locations

2 sites across 1 country: China

Source: ClinicalTrials.gov record NCT06245785. Inclusion in this directory is not an endorsement.