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:
2025-12-24 @ 6:50 PM
Ignite Modification Date:
2025-12-24 @ 6:50 PM
NCT ID:
NCT02018757
Eligibility Criteria:
Inclusion Criteria:
* accordance with primary hepatocellular carcinoma diagnosis standard：cytohistology standard or non-invasive standard.1）+2）a or 1）+2）b+3）of the following are the non-invasive diagnosis criteria:(1)patients with HBV or HCV related liver cirrhosis.(2)radiological lesion(s) in liver with arterial hypervascularity and venous or delayed phase washout: a.one kind of imaging technology diagnosis for those with lesions\>2cm;b.two kinds of imaging technology obtains the consistent conclusion for lesions with diameter of 1-2 cm.(3)serum AFP level ≥400 ug/L lasting for more than 1 month or ≥200 ug/L lasting for more than 2 months, other diseases that may cause the AFP level increase can be excluded,such as pregnancy, genital or embryonic tumors and active hepatitis.
* age of 18 to 75 year,male or female
* life expectancy of 12 weeks
* Barcelona Clinic Liver Cancer (BCLC)stage B
* laboratory tests:(1)leukocyte\>3\*19\^9/L;(2)hemoglobin≥8.5g/dl;(3)platelet count ≥50\*10\^9/L,(4)ALT and AST were less than three times the normal limit;(5)albumin ≥ 3.0 g/dl;(6)total bilirubin acuities 3 mg/dl;(7)prothrombin time international standardization ratio (PT - INR) \< = 2.3 or prothrombin time (PT)more than normal compared 3 seconds;(8)serum creatinine is less than 1.5 times the normal of the upper limit
* patients with signed informed consent
Exclusion Criteria:
* concomitant malignancies distinct from HCC currently or previously
* allergic to subject agent(such as arsenic) or other agent related to the trial
* BCLC stage 0,A,C or D
* HCC accounting for the 70% of the liver size or more
* liver function Child-Pugh score of C
* ECOG score of 1 or higher
* severe heart diseases,such as congestive heart failure with cardiac function of New York Heart Association(NYHA)functional class II or severe, active coronary disease(except for who with myocardial infarction for more than 6 months) and cardiac arrhythmia needing medical management(except for that controllable by β-blockers、calcium channel blockers and digoxin )
* uncontrollable hypertension(diastolic blood pressure cannot be controlled below 90 mmHg even after antihypertension treatment by antihypertensive drugs).
* active severe infection(grade 2 or higher according to NCI-CTCAE version 4.0)
* active tuberculosis or pulmonary tuberculosis cannot be excluded
* CNS malignancies, including intracranial metastases
* gastrointestinal bleeding with clinical findings in the previous 30 days
* chronic renal failure
* pregnancy or breastfeeding
* any other unstable conditions or circumstances possibly to jeopardise the safety or compliance of the subjects.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
75 Years
Study:
NCT02018757
Study Brief:
Protocol Section:
NCT02018757