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Balloon-Occluded Transcatheter Arterial Chemoembolization for Unresectable Primary Liver Cancer

Balloon-Occluded Transcatheter Arterial Chemoembolization for Unresectable Primary Liver Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100051432
Enrollment
Unknown
Registered
2021-09-23
Start date
2021-12-01
Completion date
Unknown
Last updated
2022-06-20

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

Conditions

primary liver cancer

Interventions

Experimental group:balloon-occuluded TACE

Sponsors

Shaanxi Provincial Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. The subjects were informed and signed the informed consent form approved by the ethics committee; 2. Aged 18 to 75 years; 3. Primary hepatocellular carcinoma diagnosed according to the diagnostic criteria for liver cancer in the guidelines for the diagnosis and treatment of primary liver cancer promulgated by the National Health and Family Planning Commission in 2019; 4. The Chinese liver cancer stage is IIa-IIIa in the 2019 edition of the Chinese Standards for the Diagnosis and Treatment of Primary Liver Cancer; 5. Good liver function (Child-Pugh A or B7 grade) or ALBI grade 1/2; 6. Performance status ECOG score of 0 or 1.

Exclusion criteria

Exclusion criteria: 1. Extrahepatic metastasis occurs; 2. Any contraindications to transarterial chemoembolization; 3. Advanced liver disease (bilirubin>2.5mg/dl, transaminase>5 times the upper limit of normal); 4. Renal failure or renal insufficiency (creatinine>2mg/L); 5. The subject is unable to perform MRI examination; 6. Pregnant, lactating women or subjects who plan to become pregnant during treatment and within 12 months after the end of treatment; 7. Women of childbearing age cannot receive reliable contraception during treatment and within 12 months after treatment; 8. The subject is currently participating in the clinical research of other experimental drugs or devices; 9. The investigator believes that the patient is not suitable to participate in this study.

Design outcomes

Primary

MeasureTime frame
Overall response rate;

Secondary

MeasureTime frame
disease-free time;overall survival;

Countries

China

Contacts

Public ContactLi Zhubin

Shaanxi Provincial Cancer Hospital

xihuan-aa@163.com+86 13759887494

Outcome results

None listed

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