Informatie:
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ID
43820
Beschrijving
Study to Evaluate the Treatment for Chronic Hepatitis C With Normal Transaminases in HIV Positive Patients; ODM derived from: https://clinicaltrials.gov/show/NCT01684787
Link
https://clinicaltrials.gov/show/NCT01684787
Trefwoorden
Versies (2)
- 03-02-17 03-02-17 -
- 20-09-21 20-09-21 -
Geüploaded op
20 september 2021
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Chronic Hepatitis C NCT01684787
Eligibility Chronic Hepatitis C NCT01684787
- StudyEvent: Eligibility
Similar models
Eligibility Chronic Hepatitis C NCT01684787
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Age
Item
patients over 18 years old
boolean
C0001779 (UMLS CUI [1])
HCV coinfection HIV-1 Stable | Alanine aminotransferase normal | Alanine aminotransferase increased
Item
hepatitis c co infected with stable hiv-1 and normal alt (case) or elevated levels of alt (control)
boolean
C1698259 (UMLS CUI [1,1])
C0019704 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
C0855620 (UMLS CUI [2])
C0151905 (UMLS CUI [3])
C0019704 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
C0855620 (UMLS CUI [2])
C0151905 (UMLS CUI [3])
CD4 Count
Item
cd4 > 200 cel/ml
boolean
C0243009 (UMLS CUI [1])
Antiretroviral therapy Stable HIV Infection
Item
stable anti-retroviral treatment for hiv during at least, the 6 previous months to the inclusion
boolean
C1963724 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
C0019693 (UMLS CUI [1,3])
C0205360 (UMLS CUI [1,2])
C0019693 (UMLS CUI [1,3])
Contraceptive methods Test Negative
Item
negative contraception test
boolean
C0700589 (UMLS CUI [1,1])
C0456984 (UMLS CUI [1,2])
C1513916 (UMLS CUI [1,3])
C0456984 (UMLS CUI [1,2])
C1513916 (UMLS CUI [1,3])
Informed Consent
Item
informed consent signed
boolean
C0021430 (UMLS CUI [1])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Therapeutic procedure Chronic Hepatitis C
Item
any previous treatment for chc
boolean
C0087111 (UMLS CUI [1,1])
C0524910 (UMLS CUI [1,2])
C0524910 (UMLS CUI [1,2])
Therapies, Investigational
Item
any experimental treatment in the 6 previous weeks to the inclusion
boolean
C0949266 (UMLS CUI [1])
Liver Cirrhosis Child-Pugh Classification
Item
cirrhosis grade b or c (child-pugh)
boolean
C0023890 (UMLS CUI [1,1])
C4050412 (UMLS CUI [1,2])
C4050412 (UMLS CUI [1,2])
Colony-Stimulating Factors | Didanosine | Zidovudine | Immunomodulators | isoniazid | Rifampin
Item
treatment with colony-stimulating factors, didanosine or zidovudine, immunomodulator therapy, isoniazid, rifampicin, …
boolean
C0009392 (UMLS CUI [1])
C0012133 (UMLS CUI [2])
C0043474 (UMLS CUI [3])
C1527392 (UMLS CUI [4])
C0022209 (UMLS CUI [5])
C0035608 (UMLS CUI [6])
C0012133 (UMLS CUI [2])
C0043474 (UMLS CUI [3])
C1527392 (UMLS CUI [4])
C0022209 (UMLS CUI [5])
C0035608 (UMLS CUI [6])
Malignant neoplasm of liver
Item
hepatic cancer
boolean
C0345904 (UMLS CUI [1])
Absolute neutrophil count | Platelet Count measurement | Hemoglobin measurement | Gender
Item
neutrophils < 1500 cel/ml, platelets < 70000 cel/ml, hemoglobin < 11 g/dl (men) or < 12 g/dl (women) previous to inclusion
boolean
C0948762 (UMLS CUI [1])
C0032181 (UMLS CUI [2])
C0518015 (UMLS CUI [3])
C0079399 (UMLS CUI [4])
C0032181 (UMLS CUI [2])
C0518015 (UMLS CUI [3])
C0079399 (UMLS CUI [4])
Mental Disorders, Severe
Item
severe psychiatric illness background
boolean
C4046029 (UMLS CUI [1])
Creatinine measurement, serum
Item
serum creatinin > 1,5 times the upper normal limit
boolean
C0201976 (UMLS CUI [1])
Lung disease | Cardiovascular Disease
Item
background of pulmonary or cardiovascular disease
boolean
C0024115 (UMLS CUI [1])
C0007222 (UMLS CUI [2])
C0007222 (UMLS CUI [2])