Hepatitis C, Chronic | HCV viral load
Item
have a clinical diagnosis of chronic hep c established on the basis of detectable viral load, as measured by a serum hcv rna test during the screening period.
boolean
C0524910 (UMLS CUI [1])
C1868902 (UMLS CUI [2])
Interferon-alpha Unresponsive to Treatment
Item
have previously failed to respond to treatment with any interferon alfa (ifna) product
boolean
C0002199 (UMLS CUI [1,1])
C0205269 (UMLS CUI [1,2])
Compensated liver disease | White Blood Cell Count procedure | Absolute neutrophil count | Platelet Count measurement | Hemoglobin | Gender
Item
have compensated liver disease with the following minimum criteria: white blood cell count > 3,000/mm3, absolute neutrophil count (anc) > 2,000/mm3, platelets > 125,000/mm3, and hemoglobin (hb) > 13 g/dl for males or > 12 g/dl for females.
boolean
C3839044 (UMLS CUI [1])
C0023508 (UMLS CUI [2])
C0948762 (UMLS CUI [3])
C0032181 (UMLS CUI [4])
C0019046 (UMLS CUI [5])
C0079399 (UMLS CUI [6])
Exclusion Criteria Major
Item
major exclusion criteria:
boolean
C0680251 (UMLS CUI [1,1])
C0205164 (UMLS CUI [1,2])
Decompensated cirrhosis Evidence of | Portal Hypertension Evidence of
Item
evidence of decompensated cirrhosis or portal hypertension.
boolean
C1619727 (UMLS CUI [1,1])
C0332120 (UMLS CUI [1,2])
C0020541 (UMLS CUI [2,1])
C0332120 (UMLS CUI [2,2])
Pregnancy | Breast Feeding
Item
pregnant or lactating female.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Disease Patient Inappropriate Clinical Trial | Condition Patient Inappropriate Clinical Trial
Item
history of any other medical disease or condition that would make the subject (in the opinion of the investigator) unsuitable for the study.
boolean
C0012634 (UMLS CUI [1,1])
C0030705 (UMLS CUI [1,2])
C1548788 (UMLS CUI [1,3])
C0008976 (UMLS CUI [1,4])
C0348080 (UMLS CUI [2,1])
C0030705 (UMLS CUI [2,2])
C1548788 (UMLS CUI [2,3])
C0008976 (UMLS CUI [2,4])
Substance Dependence
Item
a current drug or alcohol addiction
boolean
C0038580 (UMLS CUI [1])