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:
NCT03195634
Eligibility Criteria:
Inclusion Criteria:
1. Patients agreed to sign the informed consents
2. Patients aged 18-80 years,males or females
3. Patients with liver cirrhosis was diagnosed by previous liver biopsy or by compatible clinical, biochemical, and ultrasonographic/CT/MRI findings.
4. Patients were not treated with nonselective β-blockers(propranolol or carvedilol ) within previous 3 months
Exclusion Criteria:
1. Uncontrolled hypertension, diabetes or other serious cardiac problems（NYHA class IV）and pulmonary disease
2. Severe renal function injury(serum creatinine≥1.2 fold of upper limits of normal)
3. Conformed or highly suspicious diagnosis of liver malignant tumors or concomitant disease with reduced life expectancy
4. Acute hepatic failure or acute on chronic liver failure(ACLF)
5. Human immunodeficiency virus(HIV) infection
6. Previous portosystemic shunt
7. After liver transplantation
8. Pregnancy and breastfeeding
9. With contraindications of intervention surgery(hypersensitivity to iodinated contrast media, puncture site infection, severe coagulation defects, uncontrolled hyperthyroidism and multiple myeloma)
10. Participated in other drug clinical trails within 3 months
11. The researchers thought it was not suitable for this clinical trail
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
80 Years
Study:
NCT03195634
Study Brief:
Protocol Section:
NCT03195634