Informed consent
Item
given written informed consent
boolean
C0021430 (UMLS CUI [1])
Age
Item
aged 19 - 65 years
boolean
C0001779 (UMLS CUI [1])
Hepatitis B Transplantation of liver Expected
Item
expected liver transplantation related to hepatitis b
boolean
C0019163 (UMLS CUI [1,1])
C0023911 (UMLS CUI [1,2])
C1517001 (UMLS CUI [1,3])
Hepatitis B surface antigen positive
Item
positive hbsag
boolean
C0149709 (UMLS CUI [1])
Study Subject Participation Status
Item
patients has participated in any other clinical trial within 30 days
boolean
C2348568 (UMLS CUI [1])
Repeat Surgery Scheduled Transplantation of liver
Item
patients who are scheduled re-operation for liver transplantation
boolean
C0035110 (UMLS CUI [1,1])
C0205539 (UMLS CUI [1,2])
C0023911 (UMLS CUI [1,3])
Coinfection Hepatitis A Virus | HCV coinfection | Coinfection HIV
Item
patients with are co-infected with hav, hcv or hiv
boolean
C0275524 (UMLS CUI [1,1])
C0376325 (UMLS CUI [1,2])
C1698259 (UMLS CUI [2])
C0275524 (UMLS CUI [3,1])
C0019682 (UMLS CUI [3,2])
Malignant Neoplasms | Primary malignant neoplasm of liver
Item
history of malignant tumor within 5 years except primary liver cancer
boolean
C0006826 (UMLS CUI [1])
C0024620 (UMLS CUI [2])
Moderate or Severe Renal Disease | Creatinine measurement, serum | Anuria | Kidney Failure, Acute | Dialysis procedure
Item
patients with moderate or severe renal disorder (serum creatinine > 1.5 x ulm) or anuria, acute renal failure or dialysis
boolean
C3829820 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
C0003460 (UMLS CUI [3])
C0022660 (UMLS CUI [4])
C0011946 (UMLS CUI [5])
cardiovascular; attack | Myocardial Infarction | Percutaneous Transluminal Coronary Angioplasty | Coronary Artery Bypass Surgery | Angina Pectoris | Cardiac Arrhythmia | Heart valve disease | Cerebral Infarction | Cerebral Hemorrhage
Item
patients who had experienced cardiovascular attack, myocardiac infarction, ptca or coronary bypass or with angina, arrhythmia, or any other clinically meaningful valvular heart disease, cerebral infarction or cerebral hemorrhage within 6 months
boolean
C1385306 (UMLS CUI [1])
C0027051 (UMLS CUI [2])
C2936173 (UMLS CUI [3])
C0010055 (UMLS CUI [4])
C0002962 (UMLS CUI [5])
C0003811 (UMLS CUI [6])
C0018824 (UMLS CUI [7])
C0007785 (UMLS CUI [8])
C2937358 (UMLS CUI [9])
anaphylaxis Investigational New Drugs Pharmaceutical Excipient
Item
history of anaphylaxis against active ingredient or excipients of study drug
boolean
C0002792 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C0015237 (UMLS CUI [1,3])
Attenuated Vaccines Parenteral Vaccinated | Measles Vaccine | Mumps Vaccine | Rubella virus vaccine | Cholera Vaccine | Chickenpox Vaccine
Item
patients who had been vaccinated with parenteral live vaccine (measles vaccine, epidemic parotitis vaccine, rubella vaccine, cholera vaccine, chickenpox vaccine) within 3 months
boolean
C0042211 (UMLS CUI [1,1])
C1518896 (UMLS CUI [1,2])
C1519885 (UMLS CUI [1,3])
C0025010 (UMLS CUI [2])
C0026782 (UMLS CUI [3])
C0035923 (UMLS CUI [4])
C0008359 (UMLS CUI [5])
C0078048 (UMLS CUI [6])
Immunoglobulins Other
Item
patients who had been treated with any other immuno globulin within 3 months
boolean
C0021027 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
pregnant or breast-feeding women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Childbearing Potential Unwilling Contraceptive methods | Female Condom | Intrauterine Devices | Contraceptives, Oral, Hormonal | Vasectomy Sexual Partners Males
Item
women of childbearing potential who do not agree to use appropriate contraceptive methods (condom, an intrauterine device, oral contraceptive hormones, or a vasectomy of male sex partner) during this study
boolean
C3831118 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
C0700589 (UMLS CUI [1,3])
C0221829 (UMLS CUI [2])
C0021900 (UMLS CUI [3])
C0009907 (UMLS CUI [4])
C0042387 (UMLS CUI [5,1])
C0036911 (UMLS CUI [5,2])
C0086582 (UMLS CUI [5,3])
Substance Use Disorders
Item
alcohol or drug abuse within 6 months
boolean
C0038586 (UMLS CUI [1])
Disease Study Subject Participation Status Limited
Item
patients who has any clinically meaningful disease in investigator's judgement to prevent participating in this study
boolean
C0012634 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,3])