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Comparison of different carriers of DEB-TACE in the treatment of primary hepatocellular carcinoma

Comparison of different carriers of DEB-TACE in the treatment of primary hepatocellular carcinoma

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100044528
Enrollment
Unknown
Registered
2021-03-23
Start date
2021-03-25
Completion date
Unknown
Last updated
2021-09-20

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

Conditions

primary hepatocellular carcinoma

Interventions

C-TACE:Iodized oil-TACE
CalliSphere-TACE:CalliSphere-TACE
HepaSphere-TACE:HepaSphere-TACE

Sponsors

The Second Affiliated Hospital of Harbin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.The patient was over 18 years old; 2.Primary HCC patients diagnosed by histology; 3.Patients with child-Pugh A or B, BCLC stage A or B, ECOG score 0-2, and no TACE related contraindications.

Exclusion criteria

Exclusion criteria: 1.Patients who can not cooperate with follow-up information collection (such as psychiatric history, inaccurate answers); 2.Contraindications for TACE: severe liver dysfunction (child-Pugh C), including jaundice, hepatic encephalopathy, refractory ascites or hepatorenal syndrome; renal dysfunction; severe coagulation dysfunction; complete obstruction of the main portal vein with few collateral vessels; 3.Cachexia or multiple organ failure; 4.Allergic to local anesthetics, contrast agents or chemotherapy drugs; 5.Pregnant women.

Design outcomes

Primary

MeasureTime frame
RECIST;PFS;OS;OS;

Secondary

MeasureTime frame
routine blood test;Biochemical indexes;AFP;complications;

Countries

China

Contacts

Public ContactShi Zhongxing

The Second Affiliated Hospital of Harbin Medical University

975557612@qq.com+86 15104570481

Outcome results

None listed

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