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Eligibility Atrial Fibrillation NCT01198275

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
persistent atrial fibrillation (af) lasting > one month
Description

persistent atrial fibrillation

Data type

boolean

Alias
UMLS CUI [1]
C2585653
history of at least one af relapse after previous electrical or pharmacological cardioversion
Description

atrial fibrillation | Medical History, Relapse | Pharmacological cardioversion | Electric Countershock

Data type

boolean

Alias
UMLS CUI [1]
C0004238
UMLS CUI [2,1]
C0262926
UMLS CUI [2,2]
C0035020
UMLS CUI [3]
C1963873
UMLS CUI [4]
C0013778
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
left atrium size > 6 cm
Description

left atrium size

Data type

boolean

Alias
UMLS CUI [1]
C1302212
severe valvulopathy
Description

severe valvulopathy

Data type

boolean

Alias
UMLS CUI [1,1]
C0018824
UMLS CUI [1,2]
C0205082
myocardial infarction during the previous 6 months
Description

history of myocardial infarction

Data type

boolean

Alias
UMLS CUI [1]
C1275835
unstable angina
Description

unstable angina

Data type

boolean

Alias
UMLS CUI [1]
C0002965
nyha heart failure class iv or hemodynamic instability
Description

congestive heart failure, hemodynamic instability

Data type

boolean

Alias
UMLS CUI [1,1]
C0018802
UMLS CUI [1,2]
C1319796
UMLS CUI [2]
C0948268
cardiac surgery during the previous 3 months
Description

cardiac surgery

Data type

boolean

Alias
UMLS CUI [1]
C0018821
significant pulmonary thyroid and hepatic disease
Description

pulmonary thyroid and hepatic disease

Data type

boolean

Alias
UMLS CUI [1]
C0024115
UMLS CUI [2]
C0023895
UMLS CUI [3]
C0040128
contraindications to treatment with amiodarone or rass inhibitors
Description

contraindication to treatment with amiodarone or rass inhibitors

Data type

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0002598
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C3653735
chronic renal dysfunction
Description

chronic renal dysfunction

Data type

boolean

Alias
UMLS CUI [1]
C0022661
qt > 480 msec in the absence of bundle-branch block
Description

Mean QT Duration | Bundle-Branch Block

Data type

boolean

Alias
UMLS CUI [1]
C1880452
UMLS CUI [2]
C0006384
bradycardia < 50 b/min
Description

bradycardia

Data type

boolean

Alias
UMLS CUI [1]
C0428977
diagnosis of paroxysmal af
Description

paroxysmal atrial fibrillation

Data type

boolean

Alias
UMLS CUI [1]
C0235480
hyperkalemia
Description

potassium measurement

Data type

boolean

Alias
UMLS CUI [1]
C0202194
pregnancy
Description

pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
any disease or other medical treatment that, in the opinion of the investigators, could interfere with the study.
Description

Comorbidity; Limited (extensiveness); Study Protocol

Data type

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C2348563
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Similar models

Eligibility Atrial Fibrillation NCT01198275

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
persistent atrial fibrillation
Item
persistent atrial fibrillation (af) lasting > one month
boolean
C2585653 (UMLS CUI [1])
atrial fibrillation | Medical History, Relapse | Pharmacological cardioversion | Electric Countershock
Item
history of at least one af relapse after previous electrical or pharmacological cardioversion
boolean
C0004238 (UMLS CUI [1])
C0262926 (UMLS CUI [2,1])
C0035020 (UMLS CUI [2,2])
C1963873 (UMLS CUI [3])
C0013778 (UMLS CUI [4])
Item Group
C0680251 (UMLS CUI)
left atrium size
Item
left atrium size > 6 cm
boolean
C1302212 (UMLS CUI [1])
severe valvulopathy
Item
severe valvulopathy
boolean
C0018824 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
history of myocardial infarction
Item
myocardial infarction during the previous 6 months
boolean
C1275835 (UMLS CUI [1])
unstable angina
Item
unstable angina
boolean
C0002965 (UMLS CUI [1])
congestive heart failure, hemodynamic instability
Item
nyha heart failure class iv or hemodynamic instability
boolean
C0018802 (UMLS CUI [1,1])
C1319796 (UMLS CUI [1,2])
C0948268 (UMLS CUI [2])
cardiac surgery
Item
cardiac surgery during the previous 3 months
boolean
C0018821 (UMLS CUI [1])
pulmonary thyroid and hepatic disease
Item
significant pulmonary thyroid and hepatic disease
boolean
C0024115 (UMLS CUI [1])
C0023895 (UMLS CUI [2])
C0040128 (UMLS CUI [3])
contraindication to treatment with amiodarone or rass inhibitors
Item
contraindications to treatment with amiodarone or rass inhibitors
boolean
C1301624 (UMLS CUI [1,1])
C0002598 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C3653735 (UMLS CUI [2,2])
chronic renal dysfunction
Item
chronic renal dysfunction
boolean
C0022661 (UMLS CUI [1])
Mean QT Duration | Bundle-Branch Block
Item
qt > 480 msec in the absence of bundle-branch block
boolean
C1880452 (UMLS CUI [1])
C0006384 (UMLS CUI [2])
bradycardia
Item
bradycardia < 50 b/min
boolean
C0428977 (UMLS CUI [1])
paroxysmal atrial fibrillation
Item
diagnosis of paroxysmal af
boolean
C0235480 (UMLS CUI [1])
potassium measurement
Item
hyperkalemia
boolean
C0202194 (UMLS CUI [1])
pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Comorbidity; Limited (extensiveness); Study Protocol
Item
any disease or other medical treatment that, in the opinion of the investigators, could interfere with the study.
boolean
C0009488 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C2348563 (UMLS CUI [1,3])
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