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An observational multi-arm clinical trial for developing a rapid evaluation method for the applicability of unresectable HCC patients by HAIF

An observational multi-arm clinical trial for developing a rapid evaluation method for the applicability of unresectable HCC patients by HAIF

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000033734
Enrollment
Unknown
Registered
2020-06-11
Start date
2020-05-22
Completion date
Unknown
Last updated
2020-06-15

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

Conditions

Hepatacellular carcinoma

Interventions

FOLFOX:Hepatic artery perfusion FOLFOX
Combined therapy:Hepatic artery perfusion FOLFOX + other drugs or radiofrequency ablation

Sponsors

Sun Yat-sen University Cancer Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-75 years old; 2. Pathological diagnosis as HCC, or clinical imaging diagnosis as HCC; 3. At least one measurable lesion (according to mrecist); 4. Estimated survival time >=4 weeks; 5. ECOG Performance Status 0-2; 6. Child-Pugh Score A or B; 7. Leukocyte number >=3.0x10^9/l; 8. Platelet count >=50 x10^9 / L; 9. ALT and AST <=5 ULN; 10. Serum creatinine <=1.5 ULN; 11. If there is hypertension, blood pressure can be controlled; if there is diabetes, blood sugar can be controlled; 12. If you have received unexpected medication, you need to stop medication for more than 4 weeks; 13. No iodine allergy; 14. Understand the condition and sign the informed consent voluntarily

Exclusion criteria

Exclusion criteria: 1. Be allergic to the drugs which will be used; 2. If FOLFOX will be used, the patient has taken oxaliplatin, fluorouracil or folic acid; 3. Liver transplantation patients; 4. Pregnant or lactating women; 5. Uncontrollable ascites; 6. Gastroesophageal varices lead to gastrointestinal bleeding; 7. Serious hepatoencephalopathy or kidney disease, which makes it impossible to operate; 8. Serious heart disease, such as coronary artery disease, arrhythmia requiring treatment, etc; 9. There are other confirmed malignant tumors in the primary site; 10. Any unstable condition or situation that may endanger the safety and compliance of the patient.

Design outcomes

Primary

MeasureTime frame
ORR;PFS;

Countries

China

Contacts

Public ContactMing Zhao

Sun Yat-sen University Cancer Center

zhaoming@sysucc.org.cn+86 13922132569

Outcome results

None listed

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