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Transarterial chemoembolization with epirubicin-loaded CalliSpheres microspheres in the treatment of hepatocellular carcinoma: a multicenter clinical stud

Transarterial chemoembolization with epirubicin-loaded CalliSpheres microspheres in the treatment of hepatocellular carcinoma: a multicenter clinical study

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900022968
Enrollment
Unknown
Registered
2019-05-05
Start date
2019-05-06
Completion date
Unknown
Last updated
2019-05-05

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

Conditions

Liver Cancer

Interventions

case series:Transarterial chemoembolization with epirubicin-loaded CalliSpheres microspheres

Sponsors

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged between 18 to 80 years with hepatocellular carcinoma, with estimated survival time = 3 months; 2. BCLC stage B and BCLC stage A patients who are unsuitable or unwilling to undergo surgery or ablation; 3. Liver function Child-Pugh Class A or B; 4. ECOG performance status of 0 or 1; 5. patients and/or their legal representatives who agree to join the clinical trial and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Diffuse hepatocellular carcinoma; 2. Tumor burden =50% of total liver; 3. Vascular Invasion (main portal vein, primary branch of portal vein, trunk of three hepatic veins, inferior vena cava) or extrahepatic spread; 4. Severe liver function disorder (Child-Pugh grade C), including transaminase greater than 5 times the upper limit of normal, total bilirubin > 3.0 mg/dL, refractory ascites, hepatic encephalopathy or hepatorenal syndrome; 5. Uncorrectable coagulopathy; 6. White blood cell count 2 mg/dl or creatinine clearance < 30 ml/min); 9. Severe iodine contrast agent allergy; 10. Patients with dyscrasia or multiple organ failure; 11. Been received chemotherapy, ablation, transarterial embolization or chemoembolization.

Design outcomes

Primary

MeasureTime frame
progression-free survival;serious adverse events;

Countries

China

Contacts

Public ContactChuansheng Zheng

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

hqzcsxh@sina.com+86 13329702158

Outcome results

None listed

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