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A single center randomized controlled trial of CLAPT versus TACE in the treatment of advanced liver cancer complicated with portal vein tumor thrombus

A single center randomized controlled trial of CLAPT versus TACE in the treatment of advanced liver cancer complicated with portal vein tumor thrombus

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200060459
Enrollment
Unknown
Registered
2022-06-01
Start date
2022-06-06
Completion date
Unknown
Last updated
2024-05-21

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

Conditions

Advanced liver cancer complicated with portal vein tumor thrombus

Interventions

CLAPT group:CLAPT surgery + lenvatinib
TACE group:TACE+lenvatinib

Sponsors

The First Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >=18 years; 2. First confirmed advanced HCC with portal vein thrombus formation (Cheng's type ? PVTT); 3. The physical state of the eastern Tumor cooperative group (ECOG) was 0 or 1; 4. Normal liver, FLR/SLV < 30% or GRWR<0.5% by imaging examination; Abnormal liver due to obstructive jaundice, severe fatty liver, hepatitis, chemotherapy, etc., FLR/SLV < 40% or GRWR<0.8%; 5. No coagulation disorder; 6. No extrahepatic primary malignant tumor or metastasis.

Exclusion criteria

Exclusion criteria: 1. Other concurrent serious medical conditions, such as underlying heart or kidney disease, infectious diseases; 2. Pregnant and lactating patients; 3. Systemic chemotherapy and other chemotherapy treatments; 4. History of gastrointestinal bleeding within 2 weeks of enrollment.

Design outcomes

Primary

MeasureTime frame
2-year overall survival ;2-year progression-free survival;

Secondary

MeasureTime frame
Complication rates within 30 days after surgery;Mortality within 90 days after surgery;

Countries

China

Contacts

Public ContactWen Zhang
wenzgxmu@163.com+86 13878108107

Outcome results

None listed

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