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Eligibility Coronary Artery Disease NCT00290056

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
post-mi patients.
Description

Myocardial Infarction Status post

Data type

boolean

Alias
UMLS CUI [1,1]
C0027051
UMLS CUI [1,2]
C0231290
both single and dual chamber icd recipient.
Description

Single-chamber implantable defibrillator Recipient | Dual-chamber implantable defibrillator Recipient

Data type

boolean

Alias
UMLS CUI [1,1]
C3881168
UMLS CUI [1,2]
C1709854
UMLS CUI [2,1]
C0494014
UMLS CUI [2,2]
C1709854
implanted more than 3 months ago.
Description

Implantable defibrillator Implantation

Data type

boolean

Alias
UMLS CUI [1,1]
C0162589
UMLS CUI [1,2]
C0021107
agree to give written informed consent.
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
less than 18 years of age.
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
icd implantation as a `bridge` to heart transplantation.
Description

Implantable defibrillator Implantation | Heart Transplantation

Data type

boolean

Alias
UMLS CUI [1,1]
C0162589
UMLS CUI [1,2]
C0021107
UMLS CUI [2]
C0018823
stable antiarrhythmic medication over the last month prior to enrollment.
Description

Anti-Arrhythmia Agents Stable

Data type

boolean

Alias
UMLS CUI [1,1]
C0003195
UMLS CUI [1,2]
C0205360
patients taking class i antiarrhythmic medication.
Description

Anti-Arrhythmia Agents Class

Data type

boolean

Alias
UMLS CUI [1,1]
C0003195
UMLS CUI [1,2]
C0456387
a projected lifespan less than one year.
Description

Life Expectancy

Data type

boolean

Alias
UMLS CUI [1]
C0023671
participation in another trial (during or within 90 days before the study).
Description

Study Subject Participation Status

Data type

boolean

Alias
UMLS CUI [1]
C2348568
use of supplemental n-3 fatty acids during the last 3 months.
Description

Omega-3 Fatty Acids Supplemental

Data type

boolean

Alias
UMLS CUI [1,1]
C0015689
UMLS CUI [1,2]
C2348609
women who are pregnant and of childbearing potential who do not use adequate contraception.
Description

Pregnancy | Childbearing Potential Contraceptive methods Inadequate

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2,1]
C3831118
UMLS CUI [2,2]
C0700589
UMLS CUI [2,3]
C0205412
patients known to have a history of recent drug or alcohol abuse. 10) history or current intestinal or hepatic disease.
Description

Substance Use Disorders | Intestinal Disease | Liver disease

Data type

boolean

Alias
UMLS CUI [1]
C0038586
UMLS CUI [2]
C0021831
UMLS CUI [3]
C0023895
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Similar models

Eligibility Coronary Artery Disease NCT00290056

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Myocardial Infarction Status post
Item
post-mi patients.
boolean
C0027051 (UMLS CUI [1,1])
C0231290 (UMLS CUI [1,2])
Single-chamber implantable defibrillator Recipient | Dual-chamber implantable defibrillator Recipient
Item
both single and dual chamber icd recipient.
boolean
C3881168 (UMLS CUI [1,1])
C1709854 (UMLS CUI [1,2])
C0494014 (UMLS CUI [2,1])
C1709854 (UMLS CUI [2,2])
Implantable defibrillator Implantation
Item
implanted more than 3 months ago.
boolean
C0162589 (UMLS CUI [1,1])
C0021107 (UMLS CUI [1,2])
Informed Consent
Item
agree to give written informed consent.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Age
Item
less than 18 years of age.
boolean
C0001779 (UMLS CUI [1])
Implantable defibrillator Implantation | Heart Transplantation
Item
icd implantation as a `bridge` to heart transplantation.
boolean
C0162589 (UMLS CUI [1,1])
C0021107 (UMLS CUI [1,2])
C0018823 (UMLS CUI [2])
Anti-Arrhythmia Agents Stable
Item
stable antiarrhythmic medication over the last month prior to enrollment.
boolean
C0003195 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
Anti-Arrhythmia Agents Class
Item
patients taking class i antiarrhythmic medication.
boolean
C0003195 (UMLS CUI [1,1])
C0456387 (UMLS CUI [1,2])
Life Expectancy
Item
a projected lifespan less than one year.
boolean
C0023671 (UMLS CUI [1])
Study Subject Participation Status
Item
participation in another trial (during or within 90 days before the study).
boolean
C2348568 (UMLS CUI [1])
Omega-3 Fatty Acids Supplemental
Item
use of supplemental n-3 fatty acids during the last 3 months.
boolean
C0015689 (UMLS CUI [1,1])
C2348609 (UMLS CUI [1,2])
Pregnancy | Childbearing Potential Contraceptive methods Inadequate
Item
women who are pregnant and of childbearing potential who do not use adequate contraception.
boolean
C0032961 (UMLS CUI [1])
C3831118 (UMLS CUI [2,1])
C0700589 (UMLS CUI [2,2])
C0205412 (UMLS CUI [2,3])
Substance Use Disorders | Intestinal Disease | Liver disease
Item
patients known to have a history of recent drug or alcohol abuse. 10) history or current intestinal or hepatic disease.
boolean
C0038586 (UMLS CUI [1])
C0021831 (UMLS CUI [2])
C0023895 (UMLS CUI [3])
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