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NCT06609850Recruiting

The Comparison of TACE-Lenvatinib With TACE-Lenvatinib-ablation for Intermediate Recurrent Hepatocellular Carcinoma

The Comparison of TACE-Lenvatinib With TACE-Lenvatinib-ablation for Intermediate Recurrent Hepatocellular Carcinoma: a Multicenter Randomized Control Study

Source: ClinicalTrials.gov · Last updated 3 Dec 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Studies have shown that combination therapy of TACE with Lenvatinib could achieve better survival outcomes than TACE alone for hepatocellular carcinoma (HCC) at BCLC B stage. However, whether patients could benefit from the ablation for intermediate recurrent HCC (RHCC) is still need high quality clinical evidence. This study is to evaluate the efficacy of ablation combined with TACE and Lenvatinib for the intermediate-stage RHCC.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
116 (estimated)
First submitted
20 Sept 2024
Start date
1 Oct 2024
Primary completion date
1 Oct 2026
Lead sponsor
Sun Yat-sen University
NCT number
NCT06609850

What you commit to

  • Study type: Interventional
  • Planned participants: 116
  • From 1 Oct 2024 to the primary completion date, 1 Oct 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Age

  • under 18 years or over 75 years of age;

Other

  • primary intermediate-stage HCC;
  • RHCC with more than six tumors, or single RHCC
    • (5) RHCC \>5cm; (6) extrahepatic metastasis; (7) macrovascular tumor thrombus;

Who the study is looking for

  • 18-75 years;
  • RHCC diagnosed by imaging;
  • intermediate-stage RHCC (two to three lesions which at least one was \>3 cm in size or more than three tumors);
  • the tumor number was no more than six, and the maximum tumor diameter was ≤5 cm;
  • absence of extrahepatic metastasis or macrovascular invasion;
  • Child-Pugh class A or B;
  • TACE as initial treatment after tumor recurrence and showed no tumor progression after TACE.
  • life expectance \>3 months;

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Chinese PLA General Hospital
Coordinator of this site? Confirm its status
BeijingChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.