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Role of (LMWH) in Prevention of Thromboembolic Complication After (TACE) in Hepatocellular Carcinoma.

S

Sherief Abd-Elsalam

Status and phase

Unknown
Phase 3

Conditions

HCC

Treatments

Drug: LMWH
Procedure: TACE

Study type

Interventional

Funder types

Other

Identifiers

NCT02715492
LMWH TACE

Details and patient eligibility

About

Hepatocellular carcinoma (HCC) is a major health problem worldwide, and most cases are inoperable because of late presentation and underlying cirrhosis. It represents the fifth most common tumor in the world and the third most frequent cause of mortality amongst patients with cancer.

Due to the worldwide difficulties in finding liver for transplantation, hepatic resection (HR) represents the main stay of curative treatment for patients with HCC. Transcatheter arterial chemoembolization (TACE) is widely used as alternative treatments for unresectable HCC or for patients not eligible to be operated on .

TACE also could be an adjuvant therapy for resectable HCC patients after hepatectomy, which could prevent recurrence and improve long-term survival .

Full description

Thromboembolism is a well-recognised complication of malignant disease. Clinical manifestations vary from venous thromboembolism to disseminated intravascular coagulation and arterial embolism. Disseminated intravascular coagulation is most commonly observed in patients with haematological malignant disorders and those with wide spread metastatic cancer, whereas arterial embolism is most commonly observed in patients undergoing chemotherapy and in those with non-bacterial thrombotic endocarditis .

The goals of using antithrombotic therapy with TACE in HCC are to minimize mortality and to improve survival rate without provoking excessive bleeding.

Enrollment

40 estimated patients

Sex

All

Ages

40 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • HCC which was not amenable to surgical resection, liver transplantation or local ablative therapy.
  • The lesion had not been previously treated with surgery, radiation therapy, radiofrequency ablation, percutaneous ethanol or acetic acid injection, or cryoablation.
  • Reasonable performance status as adequate hematologic function; adequate hepatic function and adequate renal function.
  • Child-Pugh class A or B and no portal vein thrombosis.

Exclusion criteria

  • Child C patients Portal vein thrombosis

Trial design

Primary purpose

Prevention

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

40 participants in 2 patient groups

Transarterial Chemoembolization
Active Comparator group
Description:
1st group: included 20 patients with HCC treated by TACE only.
Treatment:
Procedure: TACE
TACE and LMWH
Experimental group
Description:
2nd group: included 20 patients with HCC treated by TACE and adjuvant dose of Low Molecular Weight Heparins (LMWH).
Treatment:
Procedure: TACE
Drug: LMWH

Trial contacts and locations

1

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Central trial contact

Sherief Abd-Elsalam, Lecturer

Data sourced from clinicaltrials.gov

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