ID

20343

Descripción

Study Effect of VIA-2291 on Vascular Inflammation; ODM derived from: https://clinicaltrials.gov/show/NCT00358826

Link

https://clinicaltrials.gov/show/NCT00358826

Palabras clave

Versiones (1)
  1. 20/2/17 20/2/17 -
Subido en

20 de febrero de 2017

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Coronary Artery Disease NCT00358826

Inglés

Eligibility Coronary Artery Disease NCT00358826

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
female patients are to be of non-childbearing potential
Descripción

Childbearing Potential

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3831118
patient has suffered an st elevation myocardial infarction (mi), non-st elevation mi, or unstable angina 21 days (±3 days) prior to study randomization
Descripción

ST segment elevation myocardial infarction | non-ST segment elevation myocardial infarction | Angina, Unstable

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1536220
UMLS CUI [2]
C1276061
UMLS CUI [3]
C0002965
patient has documented coronary artery disease
Descripción

Coronary Artery Disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1956346
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
renal insufficiency defined as creatinine >1.5 x upper limit of normal (uln)
Descripción

Renal Insufficiency | Creatinine measurement, serum

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1565489
UMLS CUI [2]
C0201976
cirrhosis, recent hepatitis, alt >1.5 x uln or alt > 1 x uln and at least one other liver function test
Descripción

Liver Cirrhosis | Hepatitis | Alanine aminotransferase measurement | Liver Function Tests Quantity

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0023890
UMLS CUI [2]
C0019158
UMLS CUI [3]
C0201836
UMLS CUI [4,1]
C0023901
UMLS CUI [4,2]
C1265611
uncontrolled diabetes mellitus within 1 month prior to study screening
Descripción

Diabetic - poor control

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0421258
congestive heart failure (chf) defined by the new york heart association as functional class iii or iv
Descripción

Congestive heart failure New York Heart Association Classification

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0018802
UMLS CUI [1,2]
C1275491
previous coronary artery bypass graft (cabg) surgery
Descripción

Coronary Artery Bypass Surgery

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0010055
planned additional cardiac intervention
Descripción

Intervention cardiac Additional Planned

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0184661
UMLS CUI [1,2]
C0018787
UMLS CUI [1,3]
C1524062
UMLS CUI [1,4]
C1301732
recurrence of st elevation mi, non-st elevation mi, or unstable angina less than 18 days prior to randomization
Descripción

ST segment elevation myocardial infarction Recurrence | non-ST segment elevation myocardial infarction Recurrence | Unstable Angina Recurrence

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1536220
UMLS CUI [1,2]
C0034897
UMLS CUI [2,1]
C1276061
UMLS CUI [2,2]
C0034897
UMLS CUI [3,1]
C0002965
UMLS CUI [3,2]
C0034897
current atrial fibrillation, atrial flutter, or frequent premature ventricular contractions
Descripción

Atrial Fibrillation | Atrial Flutter | Premature ventricular contractions Frequent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0004238
UMLS CUI [2]
C0004239
UMLS CUI [3,1]
C0151636
UMLS CUI [3,2]
C0332183
acetaminophen use in any form in the 7 days before enrollment
Descripción

Acetaminophen

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0000970
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Similar models

Eligibility Coronary Artery Disease NCT00358826

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Childbearing Potential
Item
female patients are to be of non-childbearing potential
boolean
C3831118 (UMLS CUI [1])
ST segment elevation myocardial infarction | non-ST segment elevation myocardial infarction | Angina, Unstable
Item
patient has suffered an st elevation myocardial infarction (mi), non-st elevation mi, or unstable angina 21 days (±3 days) prior to study randomization
boolean
C1536220 (UMLS CUI [1])
C1276061 (UMLS CUI [2])
C0002965 (UMLS CUI [3])
Coronary Artery Disease
Item
patient has documented coronary artery disease
boolean
C1956346 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Renal Insufficiency | Creatinine measurement, serum
Item
renal insufficiency defined as creatinine >1.5 x upper limit of normal (uln)
boolean
C1565489 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
Liver Cirrhosis | Hepatitis | Alanine aminotransferase measurement | Liver Function Tests Quantity
Item
cirrhosis, recent hepatitis, alt >1.5 x uln or alt > 1 x uln and at least one other liver function test
boolean
C0023890 (UMLS CUI [1])
C0019158 (UMLS CUI [2])
C0201836 (UMLS CUI [3])
C0023901 (UMLS CUI [4,1])
C1265611 (UMLS CUI [4,2])
Diabetic - poor control
Item
uncontrolled diabetes mellitus within 1 month prior to study screening
boolean
C0421258 (UMLS CUI [1])
Congestive heart failure New York Heart Association Classification
Item
congestive heart failure (chf) defined by the new york heart association as functional class iii or iv
boolean
C0018802 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
Coronary Artery Bypass Surgery
Item
previous coronary artery bypass graft (cabg) surgery
boolean
C0010055 (UMLS CUI [1])
Intervention cardiac Additional Planned
Item
planned additional cardiac intervention
boolean
C0184661 (UMLS CUI [1,1])
C0018787 (UMLS CUI [1,2])
C1524062 (UMLS CUI [1,3])
C1301732 (UMLS CUI [1,4])
ST segment elevation myocardial infarction Recurrence | non-ST segment elevation myocardial infarction Recurrence | Unstable Angina Recurrence
Item
recurrence of st elevation mi, non-st elevation mi, or unstable angina less than 18 days prior to randomization
boolean
C1536220 (UMLS CUI [1,1])
C0034897 (UMLS CUI [1,2])
C1276061 (UMLS CUI [2,1])
C0034897 (UMLS CUI [2,2])
C0002965 (UMLS CUI [3,1])
C0034897 (UMLS CUI [3,2])
Atrial Fibrillation | Atrial Flutter | Premature ventricular contractions Frequent
Item
current atrial fibrillation, atrial flutter, or frequent premature ventricular contractions
boolean
C0004238 (UMLS CUI [1])
C0004239 (UMLS CUI [2])
C0151636 (UMLS CUI [3,1])
C0332183 (UMLS CUI [3,2])
Acetaminophen
Item
acetaminophen use in any form in the 7 days before enrollment
boolean
C0000970 (UMLS CUI [1])
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