ID

44422

Description

The Effect of Probiotics (VSL) on Portal Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT01032941

Link

https://clinicaltrials.gov/show/NCT01032941

Keywords

  1. 8/28/18 8/28/18 -
  2. 9/20/21 9/20/21 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

September 20, 2021

DOI

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License

Creative Commons BY 4.0

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Eligibility Portal Hypertension NCT01032941

Eligibility Portal Hypertension NCT01032941

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
age 18-80
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
cirrhosis
Description

Liver Cirrhosis

Data type

boolean

Alias
UMLS CUI [1]
C0023890
childs-pugh class b/c
Description

Child-Pugh Classification

Data type

boolean

Alias
UMLS CUI [1]
C4050412
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
bacterial infection
Description

Bacterial Infection

Data type

boolean

Alias
UMLS CUI [1]
C0004623
grade 3-4 hepatic encephalopathy
Description

Hepatic Encephalopathy Grade

Data type

boolean

Alias
UMLS CUI [1,1]
C0019151
UMLS CUI [1,2]
C3890564
gi bleeding in the past 2 weeks
Description

Gastrointestinal Hemorrhage

Data type

boolean

Alias
UMLS CUI [1]
C0017181
hepatocellular carcinoma beyond the milan criteria
Description

Liver carcinoma | Other Coding

Data type

boolean

Alias
UMLS CUI [1]
C2239176
UMLS CUI [2]
C3846158
transjugular intrahepatic portosystemic shunt (tips), surgical shunt
Description

Transjugular intrahepatic portosystemic shunt procedure | Creation of shunt

Data type

boolean

Alias
UMLS CUI [1]
C0339897
UMLS CUI [2]
C0813207
portal vein thrombosis
Description

Portal vein thrombosis

Data type

boolean

Alias
UMLS CUI [1]
C0155773
antibiotics in the past 2 weeks
Description

Antibiotics

Data type

boolean

Alias
UMLS CUI [1]
C0003232
myocardial infarction, stroke or life-threatening arrhythmia within the last 6 months
Description

Myocardial Infarction | Cerebrovascular accident | Cardiac Arrhythmia Life Threatening

Data type

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2]
C0038454
UMLS CUI [3,1]
C0003811
UMLS CUI [3,2]
C2826244
active alcohol or illicit drug use
Description

Alcohol consumption | Illicit medication use

Data type

boolean

Alias
UMLS CUI [1]
C0001948
UMLS CUI [2]
C0281875
failure to consent to the study
Description

Informed Consent failed

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0231175

Similar models

Eligibility Portal Hypertension NCT01032941

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
age 18-80
boolean
C0001779 (UMLS CUI [1])
Liver Cirrhosis
Item
cirrhosis
boolean
C0023890 (UMLS CUI [1])
Child-Pugh Classification
Item
childs-pugh class b/c
boolean
C4050412 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Bacterial Infection
Item
bacterial infection
boolean
C0004623 (UMLS CUI [1])
Hepatic Encephalopathy Grade
Item
grade 3-4 hepatic encephalopathy
boolean
C0019151 (UMLS CUI [1,1])
C3890564 (UMLS CUI [1,2])
Gastrointestinal Hemorrhage
Item
gi bleeding in the past 2 weeks
boolean
C0017181 (UMLS CUI [1])
Liver carcinoma | Other Coding
Item
hepatocellular carcinoma beyond the milan criteria
boolean
C2239176 (UMLS CUI [1])
C3846158 (UMLS CUI [2])
Transjugular intrahepatic portosystemic shunt procedure | Creation of shunt
Item
transjugular intrahepatic portosystemic shunt (tips), surgical shunt
boolean
C0339897 (UMLS CUI [1])
C0813207 (UMLS CUI [2])
Portal vein thrombosis
Item
portal vein thrombosis
boolean
C0155773 (UMLS CUI [1])
Antibiotics
Item
antibiotics in the past 2 weeks
boolean
C0003232 (UMLS CUI [1])
Myocardial Infarction | Cerebrovascular accident | Cardiac Arrhythmia Life Threatening
Item
myocardial infarction, stroke or life-threatening arrhythmia within the last 6 months
boolean
C0027051 (UMLS CUI [1])
C0038454 (UMLS CUI [2])
C0003811 (UMLS CUI [3,1])
C2826244 (UMLS CUI [3,2])
Alcohol consumption | Illicit medication use
Item
active alcohol or illicit drug use
boolean
C0001948 (UMLS CUI [1])
C0281875 (UMLS CUI [2])
Informed Consent failed
Item
failure to consent to the study
boolean
C0021430 (UMLS CUI [1,1])
C0231175 (UMLS CUI [1,2])

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