Status:
UNKNOWN
Effectiveness of Drug Eluting TACE in Primary HCC
Lead Sponsor:
Assiut University
Conditions:
Hepatic Cell Carcinoma
Eligibility:
All Genders
18-75 years
Phase:
EARLY_PHASE1
Brief Summary
the aim of this work to compare effectiveness of drug-eluting bead trans-arterial chemo-embolization and conventional trans-arterial chemo-embolization of hepatic cell carcinoma in the aspect of (Tumo...
Detailed Description
Hepatocellular carcinoma (HCC) is the sixth most common cancer in the world and the third most common cause of cancer-related death .. With improved surveillance of patients with chronic liver disease...
Eligibility Criteria
Inclusion
- patients must be 18 to 75 years old.
- patients must be diagnosed as primary Hepatocellular carcinoma (HCC) by radiologic imaging revealed angiogenicity pattern .
- All of the patient have Child-Pugh status A or B .
- All of the patient have BCLC stage A or B.
- patients must have adequate renal and liver function accepting the maneuver.
- patients must have adequate coagulation profile (platelets count ≥ 80 000), (prothrombin concentration ≥ 70 %).
- patients must haven't previous history of resection of other ablation (alcohol, radio frequency or micro wave ablation).
Exclusion
- patients have previous history of resection of other ablation (alcohol, radio frequency or micro wave ablation).
- patients with impaired coagulation profile (platelets count \< 80 000), (prothrombin concentration \< 70 %).
- patients with decompensated liver cell failure having ascites which impedes the maneuver .
- patients with past history of reaction to the drug used in maneuver
- patients with poor image quality.
- patients with lost follow up .
Key Trial Info
Start Date :
September 1 2019
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2020
Estimated Enrollment :
75 Patients enrolled
Trial Details
Trial ID
NCT04048317
Start Date
September 1 2019
End Date
December 1 2020
Last Update
August 7 2019
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