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CBCT-guided Transcatheter Ethanol Delivery for Portal Vein Tumor Invasion using Cone Beam Computed Tomography

Transcatheter Ethanol Delivery for Portal Vein Tumor Invasion using Cone Beam Computed Tomography

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OPC-17012179
Enrollment
Unknown
Registered
2017-07-29
Start date
2015-03-01
Completion date
Unknown
Last updated
2017-08-21

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

Conditions

Hepatocellular Carcinoma

Interventions

Intervention group:Transcatheter arterial embolization with a mixture of lipiodol and ethanol for PVTT
Intervention group:traditional TACE for intrahepatic portion
Control group:Traditional TACE

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Unresectable HCC with PVTT (Vp3/Vp4); (2) No history of any disease-specific treatment including surgery in the past six months; (3) Optimal coagulation and liver function (Child-Pugh class A/B); (4) Eastern Cooperative Oncology Group (ECOG) score =2; (5) Informed consent of patient is available; (6) No serious concurrent medical illness; (7) Histologically or cytologically proved HCC except for lesions >2 cm, with typical features with one dynamic imaging technique and a-fetoprotein level > 40 ng/mL; (8) Tumor size up to 18 cm in the largest dimension; (9) Patients refused to receive sorafenib as the treatment for advanced HCC; (10) Patients allergic to ethanol should be included in the TACE group; (11) Patients had unsuccessful treated by sorafenib.

Exclusion criteria

Exclusion criteria: (1) Patients 75 years and older or less than 18 years; (2) Pregnant females with HCC; (3) History of variceal bleeding within the past 3 months; (4) Patients with active hepatitis B (HBV-DNA> 1000 copies/ml); (5) History of acute tumor rupture with hemoperitoneum; (6) Concurrent ischemic heart disease or heart failure; (7) History of hepatic encephalopathy; (8) Thrombosis of target hepatic artery.

Design outcomes

Primary

MeasureTime frame
overall survival;

Secondary

MeasureTime frame
adverse event;effective response;

Countries

China

Contacts

Public ContactZhengyin Liao

West China Hospital, Sichuan University

liaozhengyin@163.com+86 18980601132

Outcome results

None listed

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