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Study on the efficacy and safety of refined DEB-TACE in the treatment of primary liver cancer

Study on the efficacy and safety of refined DEB-TACE in the treatment of primary liver cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500106566
Enrollment
Unknown
Registered
2025-07-25
Start date
2025-07-30
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Hepatocellular carcinoma

Interventions

Test group:Refined DEB-TACE embolization therapy

Sponsors

People's Hospital of Henan Province
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients who meet the clinical diagnostic criteria of the 2024 edition of the "Guidelines for the Diagnosis and Treatment of Primary Liver Cancer" or have been diagnosed with primary liver cancer through pathology, have at least one measurable tumor lesion, and are not suitable/refuse surgical resection, liver transplantation, and ablation treatment; 2. Gender is not limited, age >= 18 years old; 3. Child Pugh A-B grade; 4. ECOG score 0-1 points; 5. No serious complications; 6. The patient's expected survival period exceeds 3 months; 7. Agree to participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Giant liver tumor (>= 60% liver volume); 2. Diffuse liver cancer patients; 3. Unstable systemic diseases or uncontrolled infections; 4. Difficult to correct renal function and coagulation dysfunction; 5. Any unstable condition or potential threat to patient safety and their compliance with the study; 6. Those who require termination of treatment due to any adverse events; 7. The patient or legal representative requests to stop treatment; 8. Due to various reasons, the treatment plan cannot be completed, or the patient is lost to follow-up; 9. The researchers believe that other patients who are not suitable to participate in this study.

Design outcomes

Primary

MeasureTime frame
Objective response rate;

Secondary

MeasureTime frame
Disease control rate;Progression-free survival;Overall survival;Safety;

Countries

China

Contacts

Public ContactGuangshao Cao

People's Hospital of Henan Province

yajuncao98@126.com+86 150 9310 3069

Outcome results

None listed

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