ID

19541

Description

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

Lien

https://clinicaltrials.gov/show/NCT01233635

Mots-clés

Versions (1)
  1. 08/01/2017 08/01/2017 -
Téléchargé le

8 janvier 2017

DOI

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Licence

Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT01233635

Anglais

Eligibility Atrial Fibrillation NCT01233635

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

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

Atrial Fibrillation | 12 lead ECG

Type de données

boolean

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

Blood Pressure

Type de données

boolean

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

Symptoms Cardiopulmonary Absent

Type de données

boolean

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

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
contraindiction to warfarin
Description

Medical contraindication Warfarin

Type de données

boolean

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

Myocardial Infarction | Myocardial Revascularization

Type de données

boolean

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

Cerebrovascular accident | Transient Ischemic Attack

Type de données

boolean

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

Congestive heart failure New York Heart Association Classification

Type de données

boolean

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

Thyroid Disease

Type de données

boolean

Alias
UMLS CUI [1]
C0040128
major hepatic dysfunction
Description

Liver Dysfunction Major

Type de données

boolean

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

Renal dysfunction

Type de données

boolean

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

Hyperkalemia

Type de données

boolean

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

Hyponatremia

Type de données

boolean

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

Anti-Arrhythmia Agents Class

Type de données

boolean

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

intolerance to Angiotensin Receptor Antagonists

Type de données

boolean

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

Medical contraindication Angiotensin Receptor Antagonists

Type de données

boolean

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

Pregnancy

Type de données

boolean

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

Childbearing Potential

Type de données

boolean

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

Age

Type de données

boolean

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

Informed Consent Unable

Type de données

boolean

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

Medical condition Etiology aspects Life Expectancy

Type de données

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C0015127
UMLS CUI [1,3]
C0023671
Retour au début de la page

Similar models

Eligibility Atrial Fibrillation NCT01233635

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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])
Retour au début de la page 

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