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Eligibility Atrial Fibrillation NCT01090362

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
prospective cohort
Description

Prospective Cohort

Data type

boolean

Alias
UMLS CUI [1]
C1709709
written informed consent
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
age 18 years and older
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
new diagnosis of non-valvular atrial fibrillation (diagnosed within the last 6 weeks) with at least one additional risk factor for stroke and regardless of therapy.
Description

Atrial Fibrillation Newly Diagnosed | Risk factors Quantity Cerebrovascular accident | Independent of Therapeutic procedure

Data type

boolean

Alias
UMLS CUI [1,1]
C0004238
UMLS CUI [1,2]
C1518321
UMLS CUI [2,1]
C0035648
UMLS CUI [2,2]
C1265611
UMLS CUI [2,3]
C0038454
UMLS CUI [3,1]
C0332291
UMLS CUI [3,2]
C0087111
retrospective validation cohort
Description

Retrospective Cohort

Data type

boolean

Alias
UMLS CUI [1]
C2985505
written informed consent
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
age 18 years and older
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
diagnosis of non-valvular af (diagnosed 6-24 months prior to enrolment) with at least one additional risk factor for stroke and regardless of therapy.
Description

Atrial Fibrillation | Risk factors Quantity Cerebrovascular accident | Independent of Therapeutic procedure

Data type

boolean

Alias
UMLS CUI [1]
C0004238
UMLS CUI [2,1]
C0035648
UMLS CUI [2,2]
C1265611
UMLS CUI [2,3]
C0038454
UMLS CUI [3,1]
C0332291
UMLS CUI [3,2]
C0087111
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
no further follow-up envisaged or possible within enrolling hospital or with associated family practitioner.
Description

Follow-up Plan Lacking

Data type

boolean

Alias
UMLS CUI [1,1]
C3274571
UMLS CUI [1,2]
C1301732
UMLS CUI [1,3]
C0332268
patients with transient af secondary to a reversible cause.
Description

Atrial Fibrillation Transitory | Atrial Fibrillation Secondary to Cause Reversible

Data type

boolean

Alias
UMLS CUI [1,1]
C0004238
UMLS CUI [1,2]
C0205374
UMLS CUI [2,1]
C0004238
UMLS CUI [2,2]
C0175668
UMLS CUI [2,3]
C0015127
UMLS CUI [2,4]
C0205343
patients recruited in controlled clinical trials.
Description

Patient Recruitment Controlled study

Data type

boolean

Alias
UMLS CUI [1,1]
C0242800
UMLS CUI [1,2]
C0681867
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Similar models

Eligibility Atrial Fibrillation NCT01090362

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Prospective Cohort
Item
prospective cohort
boolean
C1709709 (UMLS CUI [1])
Informed Consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Age
Item
age 18 years and older
boolean
C0001779 (UMLS CUI [1])
Atrial Fibrillation Newly Diagnosed | Risk factors Quantity Cerebrovascular accident | Independent of Therapeutic procedure
Item
new diagnosis of non-valvular atrial fibrillation (diagnosed within the last 6 weeks) with at least one additional risk factor for stroke and regardless of therapy.
boolean
C0004238 (UMLS CUI [1,1])
C1518321 (UMLS CUI [1,2])
C0035648 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0038454 (UMLS CUI [2,3])
C0332291 (UMLS CUI [3,1])
C0087111 (UMLS CUI [3,2])
Retrospective Cohort
Item
retrospective validation cohort
boolean
C2985505 (UMLS CUI [1])
Informed Consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Age
Item
age 18 years and older
boolean
C0001779 (UMLS CUI [1])
Atrial Fibrillation | Risk factors Quantity Cerebrovascular accident | Independent of Therapeutic procedure
Item
diagnosis of non-valvular af (diagnosed 6-24 months prior to enrolment) with at least one additional risk factor for stroke and regardless of therapy.
boolean
C0004238 (UMLS CUI [1])
C0035648 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0038454 (UMLS CUI [2,3])
C0332291 (UMLS CUI [3,1])
C0087111 (UMLS CUI [3,2])
Item Group
C0680251 (UMLS CUI)
Follow-up Plan Lacking
Item
no further follow-up envisaged or possible within enrolling hospital or with associated family practitioner.
boolean
C3274571 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,3])
Atrial Fibrillation Transitory | Atrial Fibrillation Secondary to Cause Reversible
Item
patients with transient af secondary to a reversible cause.
boolean
C0004238 (UMLS CUI [1,1])
C0205374 (UMLS CUI [1,2])
C0004238 (UMLS CUI [2,1])
C0175668 (UMLS CUI [2,2])
C0015127 (UMLS CUI [2,3])
C0205343 (UMLS CUI [2,4])
Patient Recruitment Controlled study
Item
patients recruited in controlled clinical trials.
boolean
C0242800 (UMLS CUI [1,1])
C0681867 (UMLS CUI [1,2])
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