Age
Item
18 years or older
boolean
C0001779 (UMLS CUI [1])
Hepatitis C Polymerase Chain Reaction
Item
positive diagnosis of hepatitis c, by polymerase chain reaction (pcr
boolean
C0019196 (UMLS CUI [1,1])
C0032520 (UMLS CUI [1,2])
Scheduled treatment Hepatitis C | PEG-interferon alfa | Ribavirin
Item
scheduled to start treatment of hepatitis c by peg interferon and ribavirin
boolean
C3844437 (UMLS CUI [1,1])
C0019196 (UMLS CUI [1,2])
C0907160 (UMLS CUI [2])
C0035525 (UMLS CUI [3])
Informed Consent
Item
agreeing to give a written consent to participate in this study.
boolean
C0021430 (UMLS CUI [1])
Age
Item
patients under 18 years of age
boolean
C0001779 (UMLS CUI [1])
Informed Consent Refused
Item
refusal to give a consent to participate in the study
boolean
C0021430 (UMLS CUI [1,1])
C1705116 (UMLS CUI [1,2])
Alcohol or Other Drugs use
Item
history of recreational drug or alcohol use in the preceding 6 months
boolean
C0237123 (UMLS CUI [1])
Pregnancy HCG pregnancy test
Item
pregnancy by hcg pregnancy testing which will be done prior to and monthly during the 12 month hepatitis c therapy and for 6 months following the end of treatment
boolean
C0032961 (UMLS CUI [1,1])
C0546577 (UMLS CUI [1,2])
Pregnancy, Planned
Item
plan for pregnancy during the study period
boolean
C0032992 (UMLS CUI [1])
Contraceptive methods Adherence failed
Item
failure to adhere to contraceptive methods
boolean
C0700589 (UMLS CUI [1,1])
C1510802 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,3])
HIV Infection
Item
hiv disease
boolean
C0019693 (UMLS CUI [1])
Liver Cirrhosis | Liver carcinoma | Decompensated Liver Disease | Liver diseases | Hepatitis B | Hemochromatosis | Hepatitis, Autoimmune | Hepatolenticular Degeneration
Item
evidence of cirrhosis or confirmed hepatocellular carcinoma (hcc), evidence of decompensated liver disease or presence of other liver diseases such as hepatitis b, hemochromatosis, autoimmune hepatitis and wilson disease
boolean
C0023890 (UMLS CUI [1])
C2239176 (UMLS CUI [2])
C0745744 (UMLS CUI [3])
C0023895 (UMLS CUI [4])
C0019163 (UMLS CUI [5])
C0018995 (UMLS CUI [6])
C0241910 (UMLS CUI [7])
C0019202 (UMLS CUI [8])
Adverse effects Severe Interferon | Depressive disorder Marked | Autoimmune reaction | Thyroiditis | Aplastic Anemia | Adverse effects Severe Ribavirin | Hemolysis Marked | Intolerance to Orlistat | Intolerance to placebo | Allergic Reaction | Diarrhea | Flatulence | Informed Consent Withdrawal
Item
patients will be removed from the study if they develop severe side effects to ifn (e.g marked depression, autoimmune reactions like thyroiditis, aplastic anemia..), severe side effects to ribavirin (e.g. marked hemolysis) or intolerance of orlistat/placebo (e.g. allergic reaction, diarrhea, flatulence..) and withdrawal of the consent.
boolean
C0879626 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0021747 (UMLS CUI [1,3])
C0011581 (UMLS CUI [2,1])
C1706089 (UMLS CUI [2,2])
C0443146 (UMLS CUI [3])
C0040147 (UMLS CUI [4])
C0002874 (UMLS CUI [5])
C0879626 (UMLS CUI [6,1])
C0205082 (UMLS CUI [6,2])
C0035525 (UMLS CUI [6,3])
C0019054 (UMLS CUI [7,1])
C1706089 (UMLS CUI [7,2])
C1744706 (UMLS CUI [8,1])
C0076275 (UMLS CUI [8,2])
C1744706 (UMLS CUI [9,1])
C1696465 (UMLS CUI [9,2])
C1527304 (UMLS CUI [10])
C0011991 (UMLS CUI [11])
C0016204 (UMLS CUI [12])
C0021430 (UMLS CUI [13,1])
C2349954 (UMLS CUI [13,2])