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A Clinical Randomized Control Trial of Combination TACE With and Without Low-Molecular-Weight Heparin in Hepatocellular Carcinoma

The Role of LMWH Combined With TACE in Hepatocellular Carcinoma

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-08000267
Enrollment
Unknown
Registered
2008-12-29
Start date
2008-12-01
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

Group A:hypodermic injection LMWH 4100 IU each 12 hours in 6 weeks
TACE scheme: iodine oil 1.5ml/cm diametre tumour, Epirubicin Hydrochloride injection 20mg, 5-Fu 1g, Carboplatin 150 mg.

Sponsors

Shanghai Eastern Hepatobiliary Surgery Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Adults patients with a diagnosis of HCC which is not amenable to surgical resection, liver transplantation or local ablative therapy; Without metastasis out of liver Patients must have at least one tumor lesion that meets both of the following criteria:The lesion can be accurately measured in at least one dimension according to RECIST criteria The lesion has not been previously treated with surgery, radiation therapy, radiofrequency ablation, percutaneous ethanol or acetic acid injection, or cryoablation. ECOG performance status (PS) <2 No prior targeted antiangiogenic therapy. Metronomic chemotherapies are allowed. At least 4 weeks since prior systemic chemotherapy Child-Pugh class A or B No significant renal impairment (creatinine clearance < 30 mL/minute) or patients on dialysis Ability to understand the protocol and to agree to and sign a written informed consent document

Exclusion criteria

Exclusion criteria: HBSAg(-), AFP(-). prothrombin time prolonged more than 4s. blood platelets count less than 50000/L. Renal failure requiring dialysis. Child-Pugh class C hepatic impairment. clinically significant gastrointestinal bleeding within 30 days prior to study entry. History of organ allograft. Substance abuse (current), psychological, or social conditions that may interfere with the patient's participation in the study or evaluation of the study results. Known or suspected allergy to the investigational agents or any agent given in association with this trial. Pregnant or breast-feeding patients.

Design outcomes

Primary

MeasureTime frame
Survival time;Survival time with no progress of tumour;

Secondary

MeasureTime frame
Response rate;

Countries

China

Contacts

Public ContactJiamei Yang
yang-jia-mei@163.com+86 021 81875542

Outcome results

None listed

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