ID

33282

Description

Carvedilol for Prevention of Paroxysmal Atrial Fibrillation; ODM derived from: https://clinicaltrials.gov/show/NCT01608893

Link

https://clinicaltrials.gov/show/NCT01608893

Keywords

  1. 12/4/18 12/4/18 -
  2. 12/4/18 12/4/18 -
Copyright Holder

See4 clinicaltrials.gov

Uploaded on

December 4, 2018

DOI

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License

Creative Commons BY-NC 3.0

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Eligibility Atrial Fibrillation NCT01608893

Eligibility Atrial Fibrillation NCT01608893

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
must be in sinus rhythm at enrollment
Description

Sinus rhythm

Data type

boolean

Alias
UMLS CUI [1]
C0232201
ecg documented symptomatic paf (> 2 episodes of > 15minutes duration over a 6 month period)
Description

Paroxysmal atrial fibrillation Symptomatic ECG | Episode Quantity Duration Period

Data type

boolean

Alias
UMLS CUI [1,1]
C0235480
UMLS CUI [1,2]
C0231220
UMLS CUI [1,3]
C1623258
UMLS CUI [2,1]
C0332189
UMLS CUI [2,2]
C1265611
UMLS CUI [2,3]
C0449238
UMLS CUI [2,4]
C1948053
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
af due to reversible causes
Description

Atrial Fibrillation Causes Reversible

Data type

boolean

Alias
UMLS CUI [1,1]
C0004238
UMLS CUI [1,2]
C0015127
UMLS CUI [1,3]
C0205343
contraindication or previous significant adverse reaction to beta blocker therapy
Description

Medical contraindication Adrenergic beta-1 Receptor Antagonists | Adverse reactions Adrenergic beta-1 Receptor Antagonists

Data type

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0304516
UMLS CUI [2,1]
C0559546
UMLS CUI [2,2]
C0304516
persistent af
Description

Persistent atrial fibrillation

Data type

boolean

Alias
UMLS CUI [1]
C2585653
nyha class ii or greater chf
Description

Congestive heart failure New York Heart Association Classification

Data type

boolean

Alias
UMLS CUI [1,1]
C0018802
UMLS CUI [1,2]
C1275491
lvef < or = 35%
Description

Left ventricular ejection fraction

Data type

boolean

Alias
UMLS CUI [1]
C0428772
life expectancy < 1 year
Description

Life Expectancy

Data type

boolean

Alias
UMLS CUI [1]
C0023671
geographic isolation
Description

Isolation Geographic

Data type

boolean

Alias
UMLS CUI [1,1]
C0205409
UMLS CUI [1,2]
C1517526
unable to give informed consent
Description

Informed Consent Unable

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582

Similar models

Eligibility Atrial Fibrillation NCT01608893

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Sinus rhythm
Item
must be in sinus rhythm at enrollment
boolean
C0232201 (UMLS CUI [1])
Paroxysmal atrial fibrillation Symptomatic ECG | Episode Quantity Duration Period
Item
ecg documented symptomatic paf (> 2 episodes of > 15minutes duration over a 6 month period)
boolean
C0235480 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
C1623258 (UMLS CUI [1,3])
C0332189 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0449238 (UMLS CUI [2,3])
C1948053 (UMLS CUI [2,4])
Item Group
C0680251 (UMLS CUI)
Atrial Fibrillation Causes Reversible
Item
af due to reversible causes
boolean
C0004238 (UMLS CUI [1,1])
C0015127 (UMLS CUI [1,2])
C0205343 (UMLS CUI [1,3])
Medical contraindication Adrenergic beta-1 Receptor Antagonists | Adverse reactions Adrenergic beta-1 Receptor Antagonists
Item
contraindication or previous significant adverse reaction to beta blocker therapy
boolean
C1301624 (UMLS CUI [1,1])
C0304516 (UMLS CUI [1,2])
C0559546 (UMLS CUI [2,1])
C0304516 (UMLS CUI [2,2])
Persistent atrial fibrillation
Item
persistent af
boolean
C2585653 (UMLS CUI [1])
Congestive heart failure New York Heart Association Classification
Item
nyha class ii or greater chf
boolean
C0018802 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
Left ventricular ejection fraction
Item
lvef < or = 35%
boolean
C0428772 (UMLS CUI [1])
Life Expectancy
Item
life expectancy < 1 year
boolean
C0023671 (UMLS CUI [1])
Isolation Geographic
Item
geographic isolation
boolean
C0205409 (UMLS CUI [1,1])
C1517526 (UMLS CUI [1,2])
Informed Consent Unable
Item
unable to give informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])

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