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DEB-TACE compared with Conventional-TACE for hepatocellular carcinoma: a prospective randomized controlled study

DEB-TACE compared with Conventional-TACE for hepatocellular carcinoma: a prospective randomized controlled study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-15006999
Enrollment
Unknown
Registered
2015-08-25
Start date
2015-09-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

hepatocellular carcinoma

Interventions

1-BCLC B:DEB-TACE
1-BCLC C:DEB-TACE
2-BCLC B:C-TACE
2-BCLC C:C-TACE

Sponsors

the Third Affiliated Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Clinical or pathological diagnosis of hepatocellular carcinoma; 2. The maximum diameter of the tumors are less than 10cm, diagnosis of BCLC stage B or C; 3. Child-Pugh level A or B, ECOG performance status of 0-2; 4. Be able to follow the visit/treatment rules according to the research programs.

Exclusion criteria

Exclusion criteria: 1. Extrahepatic metastasis; 2. Tumor thrombis invase main portal vein; 3. Patients with previously/future surgery, local-regional therapies (radiofrequency ablation, et al), or liver transplantation; 4. Patients with previously/future sorafenib therapy, systemic chemotherapy, intra-arterial chemoinfusion; 5. Had other serious medical comorbidities.

Design outcomes

Primary

MeasureTime frame
Oversurvival;Time to progression;

Secondary

MeasureTime frame
Life Quality;

Countries

China

Contacts

Public ContactMingsheng Huang, Hong Shan
gzhuangms@163.com+86 020-85252066

Outcome results

None listed

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