Age | Chronic Hepatitis C Genotype | Transplantation of liver Cadaver donor | Transplantation of liver Living Donor
Item
patient ≥ 18 years of age with documented chronic hepatitis c virus infection of genotype 1a undergoing liver transplantation from either a deceased donor or living donor.
boolean
C0001779 (UMLS CUI [1])
C0524910 (UMLS CUI [2,1])
C1533728 (UMLS CUI [2,2])
C0023911 (UMLS CUI [3,1])
C0524354 (UMLS CUI [3,2])
C0023911 (UMLS CUI [4,1])
C0348050 (UMLS CUI [4,2])
Informed Consent | Informed Consent Guardian | Informed Consent Patient Representative
Item
patient or legal guardian/health care proxy must have read, understood and provided written informed consent and hipaa authorization after the nature of the study has been fully explained.
boolean
C0021430 (UMLS CUI [1])
C0021430 (UMLS CUI [2,1])
C1274041 (UMLS CUI [2,2])
C0021430 (UMLS CUI [3,1])
C0030701 (UMLS CUI [3,2])
Serology positive Hepatitis B Surface Antigens
Item
positive serology for hepatitis b surface antigen
boolean
C0242089 (UMLS CUI [1,1])
C0019168 (UMLS CUI [1,2])
HIV Seropositivity
Item
positive serology for hiv
boolean
C0019699 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
pregnancy or breastfeeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Organ Transplantation
Item
previous history of any organ transplant
boolean
C0029216 (UMLS CUI [1])
Organ Transplantation Combined Planned | Liver Kidney Transplantation
Item
planned receipt of combined organ transplant (e.g. liver and kidney)
boolean
C0029216 (UMLS CUI [1,1])
C0205195 (UMLS CUI [1,2])
C1301732 (UMLS CUI [1,3])
C0023884 (UMLS CUI [2,1])
C0022646 (UMLS CUI [2,2])
C0040732 (UMLS CUI [2,3])
Immunoglobulin, Intravenous | Intravenous Immunoglobulin Planned
Item
receipt or planned receipt of immune globulin (ivig) within 90 days of enrollment
boolean
C0085297 (UMLS CUI [1])
C0085297 (UMLS CUI [2,1])
C1301732 (UMLS CUI [2,2])
Malignant Neoplasms Extrahepatic | Chemotherapy | Exception Chemoembolization Liver carcinoma
Item
history of extrahepatic malignancy and/or receiving chemotherapy within 90 days prior to enrollment with the exception of chemoembolization for hepatocellular carcinoma
boolean
C0006826 (UMLS CUI [1,1])
C1517058 (UMLS CUI [1,2])
C0392920 (UMLS CUI [2])
C1705847 (UMLS CUI [3,1])
C0796679 (UMLS CUI [3,2])
C2239176 (UMLS CUI [3,3])
Liver carcinoma | Tumor Burden | Criteria Specified failed
Item
hepatocellular carcinoma with tumor burden outside of the milan criteria
boolean
C2239176 (UMLS CUI [1])
C1449699 (UMLS CUI [2])
C0243161 (UMLS CUI [3,1])
C0205369 (UMLS CUI [3,2])
C0231175 (UMLS CUI [3,3])
Chronic Kidney Insufficiency | Creatinine measurement, serum
Item
history of chronic renal insufficiency or creatinine > 2.5 for ≥ six months
boolean
C0403447 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
History of Deep vein thrombosis | Family history Deep Vein Thrombosis | Personal history of pulmonary embolism | Family history of pulmonary embolism
Item
personal or family history of deep venous thrombosis or pulmonary embolism
boolean
C0459853 (UMLS CUI [1])
C0241889 (UMLS CUI [2,1])
C0149871 (UMLS CUI [2,2])
C0585968 (UMLS CUI [3])
C2317597 (UMLS CUI [4])
Allograft liver Recipient | Donor Hepatitis C Virus Positive | Donor Hepatitis B core antibody positive
Item
receipt of liver allograft from hcv positive donor or hepatitis b core antibody positive donor
boolean
C1720451 (UMLS CUI [1,1])
C1709854 (UMLS CUI [1,2])
C0029206 (UMLS CUI [2,1])
C4330254 (UMLS CUI [2,2])
C0029206 (UMLS CUI [3,1])
C0262506 (UMLS CUI [3,2])
Allograft liver Recipient | Status post Cardiac Death Donor
Item
receipt of liver allograft donated after cardiac death of donor
boolean
C1720451 (UMLS CUI [1,1])
C1709854 (UMLS CUI [1,2])
C0231290 (UMLS CUI [2,1])
C0376297 (UMLS CUI [2,2])
C0029206 (UMLS CUI [2,3])
Antiviral Agents Hepatitis C virus | Antiviral Agents Investigational Hepatitis C virus
Item
receipt of any antiviral agents, licensed or investigational for hepatitis c virus within 90 days prior to enrollment
boolean
C0003451 (UMLS CUI [1,1])
C0220847 (UMLS CUI [1,2])
C0003451 (UMLS CUI [2,1])
C1517586 (UMLS CUI [2,2])
C0220847 (UMLS CUI [2,3])
Investigational New Drugs
Item
receipt of any other investigational study product within 30 days prior to enrollment
boolean
C0013230 (UMLS CUI [1])
Condition compromises Patient safety | Condition compromises Patient Rights | Patient condition Completion of clinical trial Unlikely
Item
any other condition that in the opinion of the investigator would jeopardize the safety or rights of the patient participating in the study or make it unlikely that the patient could complete the study
boolean
C0348080 (UMLS CUI [1,1])
C2945640 (UMLS CUI [1,2])
C1113679 (UMLS CUI [1,3])
C0348080 (UMLS CUI [2,1])
C2945640 (UMLS CUI [2,2])
C0030706 (UMLS CUI [2,3])
C0683521 (UMLS CUI [3,1])
C2732579 (UMLS CUI [3,2])
C0750558 (UMLS CUI [3,3])