Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 2:23 AM
Ignite Modification Date:
2025-12-25 @ 2:23 AM
NCT ID:
NCT01798134
Eligibility Criteria:
Inclusion Criteria:
1. Patients with a confirmed diagnosis of HCC according to the European Association for the Study of the Liver (EASL) criteria for diagnosis, and staged according to the Barcelona clinic liver cancer (BCLC) criteria
2. Subject is competent and willing to provide written informed consent in order to participate in the study
3. Adults (male or female) patients ≥ 18 years of age
4. Eastern Cooperative Oncology Group (ECOG) performance status 0-2 or Child Pugh classification is 0-11
5. Multidonar or single nodular tumor ≥3-10cm, Patients with bilobar disease who can be treated superselectively in a single session or both lobes able to be treated within 3-5 weeks. Patient must have at least one tumor lesion that meets the following criteria: Lesion can be accurately measured in at least one dimension according to modified Response Evaluation Criteria In Solid Tumors (mRECIST) criteria
6. No invasion in the major blood vessel (hepatic portal, hepatic vein) or bile duct by the Magnetic resonance imaging (MRI) or Computed Tomography (CT)
7. Proper blood, liver, renal, heart function: testing result within 2 weeks from registry of this study
8. No current infections requiring antibiotic therapy
9. Not actively on cumarin based anticoagulation or suffering from a known bleeding disorder
10. Measurable disease per the Response Evaluation Criteria in Solid Tumors (mRECIST)
11. Expected survival more than 6 months
Exclusion Criteria:
1. ECOG performance status \>2; or Child-Pugh class C11 or more, or ASA class 5
2. Bilirubin levels \>3 mg/dl
3. HCC with large vessel or biliary duct invasion, diffuse HCC or extrahepatic spread
4. Patients in which any of the following are contraindicated or present:
* The use of doxorubicin
* MRI
* Hepatic embolization procedures
* White blood cell (WBC) \< 3000 cells/mm3
* neutrophil \< 1500 cells/mm3
* Cardiac ejection fraction \< 50 percent assessed by isotopic ventriculography, echocardiography or MR
* Elevated creatinine greater than or equal to 2.5 mg/dl
* Impaired clotting test (platelet count \< 5 x 104/mm3, Prothrombin time-International normalized ratio (PT-INR \> 2.0)
* aspartate transaminase (AST) and/or alanine transaminase (ALT) \>5x ULN or, when greater \>250 U/L
* Known hepatofugal blood flow
* Arterio-venous shunt
* Arterio-portal shunt
* Main stem portal vein occlusion(point 6 in inclusion criteria)
5. Women who are pregnant or breast feeding
6. Allergy to iodinated contrast used for angiography
7. Tumour burden of more than 50% of liver
8. Patients with objective signs of active bacterial, viral (human immunodeficiency virus (HIV)), or fungal infection
9. Other primary malignancies or evidence of metastatic disease
10. Patients previously treated with anthracyclines (other than doxorubicin).
11. Any co-morbid disease or condition or event that, in the investigator's judgment, would place the patient at undue risk that would preclude the safe use of DEB-TACE.
12. Under no circumstances should patients be enrolled in this study who is already participating in another study for treatment of primary liver cancer.
13. Under no circumstances should patients be enrolled in this study who has received any other embolotherapy (including Selective Internal Radiation Therapy (SIRT)) for the treatment of primary liver cancer.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT01798134
Study Brief:
Protocol Section:
NCT01798134