Age | Orthotopic liver transplant Allograft Primary | Transplantation of liver Allograft Split | cirrhosis due to hepatitis C
Item
patients 18 to 65 years of age who will undergo primary orthotopic liver or split liver allograft transplantation for hcv-cirrhosis are eligible for the study.
boolean
C0001779 (UMLS CUI [1])
C0400447 (UMLS CUI [2,1])
C0040739 (UMLS CUI [2,2])
C0205225 (UMLS CUI [2,3])
C0023911 (UMLS CUI [3,1])
C0040739 (UMLS CUI [3,2])
C1534709 (UMLS CUI [3,3])
C2075271 (UMLS CUI [4])
Liver transplant recipient Cadaver donor | ABO blood type Compatible
Item
patients receiving a cadaveric liver transplant with compatible abo blood type can be included.
boolean
C3811922 (UMLS CUI [1,1])
C0524354 (UMLS CUI [1,2])
C0200499 (UMLS CUI [2,1])
C1524057 (UMLS CUI [2,2])
Recipient Transplanted organ multiple
Item
recipient of multi-organ transplant
boolean
C1709854 (UMLS CUI [1,1])
C0524930 (UMLS CUI [1,2])
C0439064 (UMLS CUI [1,3])
Recipient Heterotopic graft
Item
recipient of an auxiliary graft
boolean
C1709854 (UMLS CUI [1,1])
C0686910 (UMLS CUI [1,2])
Recipient Graft Blood type ABO incompatibility
Item
patient is receiving abo incompatible graft
boolean
C1709854 (UMLS CUI [1,1])
C0332835 (UMLS CUI [1,2])
C0238580 (UMLS CUI [1,3])
Therapeutic immunosuppression Patient need for
Item
patients requiring immunosuppressive treatment
boolean
C0021079 (UMLS CUI [1,1])
C0686904 (UMLS CUI [1,2])
Steroid therapy Patient need for
Item
patients requiring ongoing corticosteroid therapy.
boolean
C0149783 (UMLS CUI [1,1])
C0686904 (UMLS CUI [1,2])
Communicable Diseases Uncontrolled | Severe diarrhea | Vomiting | Upper Gastrointestinal Tract Malabsorption | Peptic Ulcer
Item
patient has significant, uncontrolled concomitant infections and/or severe diarrhoea, vomiting, active upper gastro-intestinal tract malabsorption or active peptic ulcer.
boolean
C0009450 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C1443924 (UMLS CUI [2])
C0042963 (UMLS CUI [3])
C3203348 (UMLS CUI [4,1])
C3714745 (UMLS CUI [4,2])
C0030920 (UMLS CUI [5])
HIV Seropositivity | Donor HIV Seropositivity
Item
patient or donor is known to be hiv positive.
boolean
C0019699 (UMLS CUI [1])
C0013018 (UMLS CUI [2,1])
C0019699 (UMLS CUI [2,2])
Hypersensitivity Investigational New Drugs | Intolerance to Investigational New Drugs
Item
patient is allergic or intolerant to study medication
boolean
C0020517 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C1744706 (UMLS CUI [2,1])
C0013230 (UMLS CUI [2,2])
Pregnancy | Breast Feeding
Item
patient is pregnant or breast-feeding.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Study Subject Participation Status
Item
patient has been previously enrolled in this study
boolean
C2348568 (UMLS CUI [1])