ID

36271

Beschrijving

Effect of Administration of Rifaximin on the Portal Pressure of Patients With Liver Cirrhosis and Esophageal Varices; ODM derived from: https://clinicaltrials.gov/show/NCT02508623

Link

https://clinicaltrials.gov/show/NCT02508623

Trefwoorden

Versies (1)
  1. 27-04-19 27-04-19 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

27 april 2019

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Liver Cirrhosis NCT02508623

Engels

Eligibility Liver Cirrhosis NCT02508623

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosis of liver cirrhosis (based on clinical, biochemical and radiological criteria with or without liver biopsy)
Beschrijving

Liver Cirrhosis | Biopsy of liver

Datatype

boolean

Alias
UMLS CUI [1]
C0023890
UMLS CUI [2]
C0193388
presence of esophageal varices at high risk of bleeding
Beschrijving

Esophageal Varices | High risk of bleeding

Datatype

boolean

Alias
UMLS CUI [1]
C0014867
UMLS CUI [2]
C4039184
hepatic venous pressure gradient > 12 mmhg.
Beschrijving

Hepatic venous pressure gradient

Datatype

boolean

Alias
UMLS CUI [1]
C4049263
19≤ age ≤75
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
informed consent
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients already treated with beta blockers
Beschrijving

Adrenergic beta-1 Receptor Antagonists

Datatype

boolean

Alias
UMLS CUI [1]
C0304516
treatment with systemic antibiotics and/or non-absorbable intestinal antibiotics in the previous two weeks
Beschrijving

Antibiotics for systemic use | Intestinal antibiotics Absorption unsuccessful

Datatype

boolean

Alias
UMLS CUI [1]
C3540704
UMLS CUI [2,1]
C3540709
UMLS CUI [2,2]
C0000854
UMLS CUI [2,3]
C1272705
bacterial infection, spontaneous bacterial peritonitis
Beschrijving

Bacterial Infection | Primary bacterial peritonitis

Datatype

boolean

Alias
UMLS CUI [1]
C0004623
UMLS CUI [2]
C0275551
overt hepatic encephalopathy in the last week
Beschrijving

Hepatic Encephalopathy

Datatype

boolean

Alias
UMLS CUI [1]
C0019151
active gastrointestinal bleeding, or in the last week
Beschrijving

Gastrointestinal Hemorrhage

Datatype

boolean

Alias
UMLS CUI [1]
C0017181
active alcoholism or drug abuse in last 3 weeks
Beschrijving

Alcoholic Intoxication, Chronic | Drug abuse

Datatype

boolean

Alias
UMLS CUI [1]
C0001973
UMLS CUI [2]
C0013146
acute alcoholic hepatitis
Beschrijving

Hepatitis, Alcoholic

Datatype

boolean

Alias
UMLS CUI [1]
C0019187
hepatocellular carcinoma or other neoplasm
Beschrijving

Liver carcinoma | Cancer Other

Datatype

boolean

Alias
UMLS CUI [1]
C2239176
UMLS CUI [2]
C1707251
significant coronary artery disease (angina nyha iii/iv), congestive heart failure (nyha iii/iv), relevant cardiomyopathy, history of myocardial infarct within the last 12 months
Beschrijving

Coronary Artery Disease | Angina Pectoris New York Heart Association Classification | Congestive heart failure New York Heart Association Classification | Cardiomyopathy | Myocardial Infarction

Datatype

boolean

Alias
UMLS CUI [1]
C1956346
UMLS CUI [2,1]
C0002962
UMLS CUI [2,2]
C1275491
UMLS CUI [3,1]
C0018802
UMLS CUI [3,2]
C1275491
UMLS CUI [4]
C0878544
UMLS CUI [5]
C0027051
contraindications to the administration of beta blockers; allergy to rifaximin
Beschrijving

Medical contraindication Adrenergic beta-1 Receptor Antagonists | Hypersensitivity Rifaximin

Datatype

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0304516
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0073374
pregnancy or breastfeeding
Beschrijving

Pregnancy | Breast Feeding

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
refusal to participate
Beschrijving

Participation Refused

Datatype

boolean

Alias
UMLS CUI [1,1]
C0679823
UMLS CUI [1,2]
C1705116
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Similar models

Eligibility Liver Cirrhosis NCT02508623

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Liver Cirrhosis | Biopsy of liver
Item
diagnosis of liver cirrhosis (based on clinical, biochemical and radiological criteria with or without liver biopsy)
boolean
C0023890 (UMLS CUI [1])
C0193388 (UMLS CUI [2])
Esophageal Varices | High risk of bleeding
Item
presence of esophageal varices at high risk of bleeding
boolean
C0014867 (UMLS CUI [1])
C4039184 (UMLS CUI [2])
Hepatic venous pressure gradient
Item
hepatic venous pressure gradient > 12 mmhg.
boolean
C4049263 (UMLS CUI [1])
Age
Item
19≤ age ≤75
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Adrenergic beta-1 Receptor Antagonists
Item
patients already treated with beta blockers
boolean
C0304516 (UMLS CUI [1])
Antibiotics for systemic use | Intestinal antibiotics Absorption unsuccessful
Item
treatment with systemic antibiotics and/or non-absorbable intestinal antibiotics in the previous two weeks
boolean
C3540704 (UMLS CUI [1])
C3540709 (UMLS CUI [2,1])
C0000854 (UMLS CUI [2,2])
C1272705 (UMLS CUI [2,3])
Bacterial Infection | Primary bacterial peritonitis
Item
bacterial infection, spontaneous bacterial peritonitis
boolean
C0004623 (UMLS CUI [1])
C0275551 (UMLS CUI [2])
Hepatic Encephalopathy
Item
overt hepatic encephalopathy in the last week
boolean
C0019151 (UMLS CUI [1])
Gastrointestinal Hemorrhage
Item
active gastrointestinal bleeding, or in the last week
boolean
C0017181 (UMLS CUI [1])
Alcoholic Intoxication, Chronic | Drug abuse
Item
active alcoholism or drug abuse in last 3 weeks
boolean
C0001973 (UMLS CUI [1])
C0013146 (UMLS CUI [2])
Hepatitis, Alcoholic
Item
acute alcoholic hepatitis
boolean
C0019187 (UMLS CUI [1])
Liver carcinoma | Cancer Other
Item
hepatocellular carcinoma or other neoplasm
boolean
C2239176 (UMLS CUI [1])
C1707251 (UMLS CUI [2])
Coronary Artery Disease | Angina Pectoris New York Heart Association Classification | Congestive heart failure New York Heart Association Classification | Cardiomyopathy | Myocardial Infarction
Item
significant coronary artery disease (angina nyha iii/iv), congestive heart failure (nyha iii/iv), relevant cardiomyopathy, history of myocardial infarct within the last 12 months
boolean
C1956346 (UMLS CUI [1])
C0002962 (UMLS CUI [2,1])
C1275491 (UMLS CUI [2,2])
C0018802 (UMLS CUI [3,1])
C1275491 (UMLS CUI [3,2])
C0878544 (UMLS CUI [4])
C0027051 (UMLS CUI [5])
Medical contraindication Adrenergic beta-1 Receptor Antagonists | Hypersensitivity Rifaximin
Item
contraindications to the administration of beta blockers; allergy to rifaximin
boolean
C1301624 (UMLS CUI [1,1])
C0304516 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0073374 (UMLS CUI [2,2])
Pregnancy | Breast Feeding
Item
pregnancy or breastfeeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Participation Refused
Item
refusal to participate
boolean
C0679823 (UMLS CUI [1,1])
C1705116 (UMLS CUI [1,2])
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