Informatie:
Fout:
ID
14212
Beschrijving
A Trial of Ribavirin in Patients With ACLF Due to Hepatitis E Virus; ODM derived from: https://clinicaltrials.gov/show/NCT01698723
Link
https://clinicaltrials.gov/show/NCT01698723
Trefwoorden
Versies (1)
- 04-04-16 04-04-16 -
Geüploaded op
4 april 2016
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Acute on Chronic Hepatic Failure NCT01698723
Eligibility Acute on Chronic Hepatic Failure NCT01698723
- StudyEvent: Eligibility
Similar models
Eligibility Acute on Chronic Hepatic Failure NCT01698723
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Acute-On-Chronic Liver Failure
Item
all aclf due to hev
boolean
C3850141 (UMLS CUI [1])
Informed Consent
Item
consent to participate in trial and collection of blood
boolean
C0021430 (UMLS CUI [1])
Patient pregnant
Item
pregnant and nursing mothers
boolean
C0549206 (UMLS CUI [1])
Anemia, severe
Item
severe anemia
boolean
C0238644 (UMLS CUI [1])
other etiologies of aclf
Item
other etiologies of aclf (eg. alcohol, drugs, reactivation of hepatitis b and hepatitis c, variceal bleeding, surgical intervention and sepsis)
boolean
C3850141 (UMLS CUI [1])
Liver carcinoma
Item
hepatocellular carcinoma (hcc)
boolean
C2239176 (UMLS CUI [1])
Hepatorenal Syndrome
Item
hepatorenal syndrome (hrs) at admission
boolean
C0019212 (UMLS CUI [1])
Life Threatening Adverse Event
Item
presence of life threatening cardiovascular, respiratory and neurological disease
boolean
C1517874 (UMLS CUI [1])
Acquired Immunodeficiency Syndrome
Item
acquired immunodeficiency syndrome
boolean
C0001175 (UMLS CUI [1])
Hemoglobinopathies
Item
patients with hemoglobinopathies (e.g., thalassemia major, sickle-cell anemia)
boolean
C0019045 (UMLS CUI [1])
participate in the study
Item
refusal to provide consent to participate in the study
boolean
C2348568 (UMLS CUI [1])