Eligibility Module

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 @ 12:52 AM
Ignite Modification Date: 2025-12-25 @ 12:52 AM
NCT ID: NCT02297867
Eligibility Criteria: Inclusion Criteria: 1. Liver cirrhosis investigators with age 20 to 80 years (both inclusive). 2. Investigators without Mandatory Communicable Disease (HBV, HCV, HIV, syphilis) 3. Investigators without rare disorder 4. Coagulation normalities 5. Investigators without autoimmune disorder 6. Investigators without Acquired Immune Deficiency Syndrome 7. Investigators without cancer 8. Investigators BMI \> 15 Exclusion Criteria: 1. Pregnant women 2. Investigators with acute stroke in one month and unconsciousness 3. Investigators with acute myocardial infarction or acute heart failure 4. Investigators with serious liver dysfunction and coagulation dysfunction and ascites mild higher 5. Investigators with acute respiratory failure or pneumonia 6. Kidney Failure: BUN \> 50 7. Anemia: Hematocrit \< 25 8. Investigators diagnosed with liver cancer or liver metastatic carcinoma 9. Investigators with liver abscess 10. Investigators with acute Hepatitis 11. Investigators with acute infective 12. Liver cirrhosis patients with HBV or HCV 13. Investigators diagnosed with carcinoma and receiving treatment 14. Investigators with Schizophrenia or melancholia 15. Investigators received serious surgical operations in 3 months 16. Investigators unable to control hypertension (SBP \> 180 mmHg, DBP \> 110 mmHg) or diabetes (AC sugar \> 200 mg/dl) 17. Others can't fit into the trial evaluate by investigator
Healthy Volunteers: False
Sex: ALL
Minimum Age: 20 Years
Maximum Age: 80 Years
Study: NCT02297867
Study Brief:
Protocol Section: NCT02297867