ID

19541

Beschrijving

Secondary Prevention of Atrial Fibrillation (Impact of Renin-Angiotensin-Aldosterone System Inhibition); ODM derived from: https://clinicaltrials.gov/show/NCT01233635

Link

https://clinicaltrials.gov/show/NCT01233635

Trefwoorden

  1. 08-01-17 08-01-17 -
Geüploaded op

8 januari 2017

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Atrial Fibrillation NCT01233635

Eligibility Atrial Fibrillation NCT01233635

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
subjects must be in atrial fibrillation confirmed by 12 lead ekg.
Beschrijving

Atrial Fibrillation | 12 lead ECG

Datatype

boolean

Alias
UMLS CUI [1]
C0004238
UMLS CUI [2]
C0430456
blood pressure > 90 mmhg
Beschrijving

Blood Pressure

Datatype

boolean

Alias
UMLS CUI [1]
C0005823
patient without cardiopulmonary symptoms
Beschrijving

Symptoms Cardiopulmonary Absent

Datatype

boolean

Alias
UMLS CUI [1,1]
C1457887
UMLS CUI [1,2]
C0553534
UMLS CUI [1,3]
C0332197
18+ years of age
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
contraindiction to warfarin
Beschrijving

Medical contraindication Warfarin

Datatype

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0043031
recent (within 6 months) mi or cardiac revascularization
Beschrijving

Myocardial Infarction | Myocardial Revascularization

Datatype

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2]
C0027056
recent (within 6 months) cva or tia
Beschrijving

Cerebrovascular accident | Transient Ischemic Attack

Datatype

boolean

Alias
UMLS CUI [1]
C0038454
UMLS CUI [2]
C0007787
nyha class iv chf
Beschrijving

Congestive heart failure New York Heart Association Classification

Datatype

boolean

Alias
UMLS CUI [1,1]
C0018802
UMLS CUI [1,2]
C1275491
active thyroid disease
Beschrijving

Thyroid Disease

Datatype

boolean

Alias
UMLS CUI [1]
C0040128
major hepatic dysfunction
Beschrijving

Liver Dysfunction Major

Datatype

boolean

Alias
UMLS CUI [1,1]
C0086565
UMLS CUI [1,2]
C0205164
renal dysfunction (>2 mg/dl)
Beschrijving

Renal dysfunction

Datatype

boolean

Alias
UMLS CUI [1]
C3279454
hyperkalemia (>4.6 meq/l)
Beschrijving

Hyperkalemia

Datatype

boolean

Alias
UMLS CUI [1]
C0020461
hyponatremia (<130 meq/l)
Beschrijving

Hyponatremia

Datatype

boolean

Alias
UMLS CUI [1]
C0020625
currently taking a vaughn-williams type i or iii antiarrhythmic drug
Beschrijving

Anti-Arrhythmia Agents Class

Datatype

boolean

Alias
UMLS CUI [1,1]
C0003195
UMLS CUI [1,2]
C2983595
history of arb intolerance
Beschrijving

intolerance to Angiotensin Receptor Antagonists

Datatype

boolean

Alias
UMLS CUI [1,1]
C1744706
UMLS CUI [1,2]
C0815017
contraindication to arb therapy
Beschrijving

Medical contraindication Angiotensin Receptor Antagonists

Datatype

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0815017
pregnancy
Beschrijving

Pregnancy

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
female of childbearing age
Beschrijving

Childbearing Potential

Datatype

boolean

Alias
UMLS CUI [1]
C3831118
age < 18 years of age
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
inability to give informed consent
Beschrijving

Informed Consent Unable

Datatype

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
other medical conditions calling 1 year survival into question
Beschrijving

Medical condition Etiology aspects Life Expectancy

Datatype

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C0015127
UMLS CUI [1,3]
C0023671

Similar models

Eligibility Atrial Fibrillation NCT01233635

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Atrial Fibrillation | 12 lead ECG
Item
subjects must be in atrial fibrillation confirmed by 12 lead ekg.
boolean
C0004238 (UMLS CUI [1])
C0430456 (UMLS CUI [2])
Blood Pressure
Item
blood pressure > 90 mmhg
boolean
C0005823 (UMLS CUI [1])
Symptoms Cardiopulmonary Absent
Item
patient without cardiopulmonary symptoms
boolean
C1457887 (UMLS CUI [1,1])
C0553534 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Age
Item
18+ years of age
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Medical contraindication Warfarin
Item
contraindiction to warfarin
boolean
C1301624 (UMLS CUI [1,1])
C0043031 (UMLS CUI [1,2])
Myocardial Infarction | Myocardial Revascularization
Item
recent (within 6 months) mi or cardiac revascularization
boolean
C0027051 (UMLS CUI [1])
C0027056 (UMLS CUI [2])
Cerebrovascular accident | Transient Ischemic Attack
Item
recent (within 6 months) cva or tia
boolean
C0038454 (UMLS CUI [1])
C0007787 (UMLS CUI [2])
Congestive heart failure New York Heart Association Classification
Item
nyha class iv chf
boolean
C0018802 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
Thyroid Disease
Item
active thyroid disease
boolean
C0040128 (UMLS CUI [1])
Liver Dysfunction Major
Item
major hepatic dysfunction
boolean
C0086565 (UMLS CUI [1,1])
C0205164 (UMLS CUI [1,2])
Renal dysfunction
Item
renal dysfunction (>2 mg/dl)
boolean
C3279454 (UMLS CUI [1])
Hyperkalemia
Item
hyperkalemia (>4.6 meq/l)
boolean
C0020461 (UMLS CUI [1])
Hyponatremia
Item
hyponatremia (<130 meq/l)
boolean
C0020625 (UMLS CUI [1])
Anti-Arrhythmia Agents Class
Item
currently taking a vaughn-williams type i or iii antiarrhythmic drug
boolean
C0003195 (UMLS CUI [1,1])
C2983595 (UMLS CUI [1,2])
intolerance to Angiotensin Receptor Antagonists
Item
history of arb intolerance
boolean
C1744706 (UMLS CUI [1,1])
C0815017 (UMLS CUI [1,2])
Medical contraindication Angiotensin Receptor Antagonists
Item
contraindication to arb therapy
boolean
C1301624 (UMLS CUI [1,1])
C0815017 (UMLS CUI [1,2])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Childbearing Potential
Item
female of childbearing age
boolean
C3831118 (UMLS CUI [1])
Age
Item
age < 18 years of age
boolean
C0001779 (UMLS CUI [1])
Informed Consent Unable
Item
inability to give informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Medical condition Etiology aspects Life Expectancy
Item
other medical conditions calling 1 year survival into question
boolean
C3843040 (UMLS CUI [1,1])
C0015127 (UMLS CUI [1,2])
C0023671 (UMLS CUI [1,3])

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