ID

23277

Beschrijving

Responsible Party: Dominik Bettinger, investigator, University Hospital Freiburg ClinicalTrials.gov Identifier: NCT01355107 History of Changes Other Study ID Numbers: HCC1 DRKS00000813 ( Registry Identifier: German Clinical Trials Register ) Study First Received: May 6, 2011 Last Updated: December 13, 2011 Comparison of Selenium Levels in HCV- Infected Patients at Different Stages of Disease ODM derived from: https://clinicaltrials.gov/ct2/show/NCT01355107

Link

https://clinicaltrials.gov/ct2/show/NCT01355107

Trefwoorden

Versies (1)
  1. 02-07-17 02-07-17 -
Geüploaded op

2 juli 2017

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Hepatitis C DRKS00000813 NCT01355107 DRKS00000813

Engels

Eligibility Hepatitis C NCT01355107 DRKS00000813

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI-1
C1512693
Ages Eligible for Study: 18 Years to 80 Years (Adult, Senior)
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
Sexes Eligible for Study: Male
Beschrijving

Gender

Datatype

boolean

Alias
UMLS CUI [1]
C0079399
Patients with chronic hepatitis c- infection: no cirrhosis of the liver (= Desmet IV), no HCC - suspected lesion in the liver
Beschrijving

Hepatitis C, Chronic

Datatype

boolean

Alias
UMLS CUI [1]
C0524910
Patients with hcv- associated cirrhosis of the liver: - cirrhosis of the liver confirmed by ultrasound, CT/MRI imaging or biopsy, all child - stages
Beschrijving

Cirrhosis of liver due to chronic hepatitis C

Datatype

boolean

Alias
UMLS CUI [1]
C3662136
Patients with hcv- associated HCC: diagnosis of HCC according to the AASLD criteria, HCC has not been treated at the time of enrollment, all BCLC- /UICC- stages.
Beschrijving

HCC due to chronic hepatitis C

Datatype

boolean

Alias
UMLS CUI [1,1]
C2239176
UMLS CUI [1,2]
C0524910
For all three groups: diagnosis of the chronic hcv- infection with virus rna and serologic parameters (anti-hcv) and abnormal liver function for more than 6 months, no antiviral treatment during the last 6 months
Beschrijving

Disease Status

Datatype

boolean

Alias
UMLS CUI [1]
C0699749
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI-1
C0680251
Healthy Volunteers
Beschrijving

Control Group

Datatype

boolean

Alias
UMLS CUI [1]
C0009932
Application of dietary supplements
Beschrijving

Dietary Supplements

Datatype

boolean

Alias
UMLS CUI [1]
C0242295
Excessive alcohol consumption
Beschrijving

Substance Use Disorder

Datatype

boolean

Alias
UMLS CUI [1]
C0038586
All other etiologies leading to a liver injury
Beschrijving

Liver Diseases

Datatype

boolean

Alias
UMLS CUI [1]
C0023895
Patients with an acute-phase- reaction, SIRS or patients in intensive care units
Beschrijving

Acute-phase-reaction, SIRS or patients in intensive care units

Datatype

boolean

Alias
UMLS CUI [1]
C0001349
UMLS CUI [2]
C0242966
UMLS CUI [3]
C0021708
Extrahepatic neoplasm
Beschrijving

Extrahepatic neoplasm

Datatype

boolean

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C1517058
Rheumatic disease apart from hcv- associated immunologic phenomena
Beschrijving

Rheumatic disease

Datatype

boolean

Alias
UMLS CUI [1]
C0035435
Diabetes mellitus I and II
Beschrijving

Diabetes mellitus

Datatype

boolean

Alias
UMLS CUI [1]
C0011849
Immunological diseases
Beschrijving

Immunological diseases

Datatype

boolean

Alias
UMLS CUI [1]
C0021053
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Similar models

Eligibility Hepatitis C NCT01355107 DRKS00000813

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Inclusion Criteria
C1512693 (UMLS CUI-1)
Age
Item
Ages Eligible for Study: 18 Years to 80 Years (Adult, Senior)
boolean
C0001779 (UMLS CUI [1])
Gender
Item
Sexes Eligible for Study: Male
boolean
C0079399 (UMLS CUI [1])
Hepatitis C, Chronic
Item
Patients with chronic hepatitis c- infection: no cirrhosis of the liver (= Desmet IV), no HCC - suspected lesion in the liver
boolean
C0524910 (UMLS CUI [1])
Cirrhosis of liver due to chronic hepatitis C
Item
Patients with hcv- associated cirrhosis of the liver: - cirrhosis of the liver confirmed by ultrasound, CT/MRI imaging or biopsy, all child - stages
boolean
C3662136 (UMLS CUI [1])
HCC due to chronic hepatitis C
Item
Patients with hcv- associated HCC: diagnosis of HCC according to the AASLD criteria, HCC has not been treated at the time of enrollment, all BCLC- /UICC- stages.
boolean
C2239176 (UMLS CUI [1,1])
C0524910 (UMLS CUI [1,2])
Disease Status
Item
For all three groups: diagnosis of the chronic hcv- infection with virus rna and serologic parameters (anti-hcv) and abnormal liver function for more than 6 months, no antiviral treatment during the last 6 months
boolean
C0699749 (UMLS CUI [1])
Item Group
Exclusion Criteria
C0680251 (UMLS CUI-1)
Control Group
Item
Healthy Volunteers
boolean
C0009932 (UMLS CUI [1])
Dietary Supplements
Item
Application of dietary supplements
boolean
C0242295 (UMLS CUI [1])
Substance Use Disorder
Item
Excessive alcohol consumption
boolean
C0038586 (UMLS CUI [1])
Liver Diseases
Item
All other etiologies leading to a liver injury
boolean
C0023895 (UMLS CUI [1])
Acute-phase-reaction, SIRS or patients in intensive care units
Item
Patients with an acute-phase- reaction, SIRS or patients in intensive care units
boolean
C0001349 (UMLS CUI [1])
C0242966 (UMLS CUI [2])
C0021708 (UMLS CUI [3])
Extrahepatic neoplasm
Item
Extrahepatic neoplasm
boolean
C0006826 (UMLS CUI [1,1])
C1517058 (UMLS CUI [1,2])
Rheumatic disease
Item
Rheumatic disease apart from hcv- associated immunologic phenomena
boolean
C0035435 (UMLS CUI [1])
Diabetes mellitus
Item
Diabetes mellitus I and II
boolean
C0011849 (UMLS CUI [1])
Immunological diseases
Item
Immunological diseases
boolean
C0021053 (UMLS CUI [1])
Terug naar het begin van de pagina 

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