ID

33279

Description

Extended Rhythm SCreening for AtRial Fibrillation in Cryptogenic Stroke Patients; ODM derived from: https://clinicaltrials.gov/show/NCT01550042

Link

https://clinicaltrials.gov/show/NCT01550042

Keywords

Versions (1)
  1. 12/4/18 12/4/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

December 4, 2018

DOI

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License

Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT01550042

English

Eligibility Atrial Fibrillation NCT01550042

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients > 18 years of age recent episode (≤60 days) of cryptogenic ischemic stroke
Description

Age | Episode of Ischemic stroke cryptogenic

Data type

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2,1]
C0332189
UMLS CUI [2,2]
C0948008
UMLS CUI [2,3]
C0332240
undetermined etiology with negative evaluation (including cardioembolism work-
Description

Etiology Undetermined | Evaluation Negative | Cardiac embolism work up

Data type

boolean

Alias
UMLS CUI [1,1]
C1314792
UMLS CUI [1,2]
C4082977
UMLS CUI [2,1]
C1261322
UMLS CUI [2,2]
C1513916
UMLS CUI [3,1]
C0442840
UMLS CUI [3,2]
C0750430
up) according to the criteria for the trial of org 10172 in acute stroke treatment (toast)
Description

TOAST Classification

Data type

boolean

Alias
UMLS CUI [1]
C1710306
implantation of an implantable loop recorder within two months after index event
Description

Implantation of insertable loop recorder

Data type

boolean

Alias
UMLS CUI [1]
C1277164
able of providing informed consent
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
pre-existing indication for vitamin k antagonist
Description

Indication Pre-existing Vitamin K Antagonist

Data type

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C2347662
UMLS CUI [1,3]
C2267235
untreated hyperthyroidism
Description

Hyperthyroidism Untreated

Data type

boolean

Alias
UMLS CUI [1,1]
C0020550
UMLS CUI [1,2]
C0332155
indication for pacemaker implantation, implantable cardioverter defibrillator (icd) or cardiac resynchronisation therapy (crt)
Description

Indication Implantation of cardiac pacemaker | Indication Implantable defibrillator | Indication Cardiac Resynchronization Therapy

Data type

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0189842
UMLS CUI [2,1]
C3146298
UMLS CUI [2,2]
C0162589
UMLS CUI [3,1]
C3146298
UMLS CUI [3,2]
C1167956
severe co-morbidity not likely to complete follow-up for one year
Description

Comorbidity Severe | Clinical Study Follow-up Completion Unlikely

Data type

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0205082
UMLS CUI [2,1]
C3274571
UMLS CUI [2,2]
C0205197
UMLS CUI [2,3]
C0750558
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Similar models

Eligibility Atrial Fibrillation NCT01550042

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age | Episode of Ischemic stroke cryptogenic
Item
patients > 18 years of age recent episode (≤60 days) of cryptogenic ischemic stroke
boolean
C0001779 (UMLS CUI [1])
C0332189 (UMLS CUI [2,1])
C0948008 (UMLS CUI [2,2])
C0332240 (UMLS CUI [2,3])
Etiology Undetermined | Evaluation Negative | Cardiac embolism work up
Item
undetermined etiology with negative evaluation (including cardioembolism work-
boolean
C1314792 (UMLS CUI [1,1])
C4082977 (UMLS CUI [1,2])
C1261322 (UMLS CUI [2,1])
C1513916 (UMLS CUI [2,2])
C0442840 (UMLS CUI [3,1])
C0750430 (UMLS CUI [3,2])
TOAST Classification
Item
up) according to the criteria for the trial of org 10172 in acute stroke treatment (toast)
boolean
C1710306 (UMLS CUI [1])
Implantation of insertable loop recorder
Item
implantation of an implantable loop recorder within two months after index event
boolean
C1277164 (UMLS CUI [1])
Informed Consent
Item
able of providing informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Indication Pre-existing Vitamin K Antagonist
Item
pre-existing indication for vitamin k antagonist
boolean
C3146298 (UMLS CUI [1,1])
C2347662 (UMLS CUI [1,2])
C2267235 (UMLS CUI [1,3])
Hyperthyroidism Untreated
Item
untreated hyperthyroidism
boolean
C0020550 (UMLS CUI [1,1])
C0332155 (UMLS CUI [1,2])
Indication Implantation of cardiac pacemaker | Indication Implantable defibrillator | Indication Cardiac Resynchronization Therapy
Item
indication for pacemaker implantation, implantable cardioverter defibrillator (icd) or cardiac resynchronisation therapy (crt)
boolean
C3146298 (UMLS CUI [1,1])
C0189842 (UMLS CUI [1,2])
C3146298 (UMLS CUI [2,1])
C0162589 (UMLS CUI [2,2])
C3146298 (UMLS CUI [3,1])
C1167956 (UMLS CUI [3,2])
Comorbidity Severe | Clinical Study Follow-up Completion Unlikely
Item
severe co-morbidity not likely to complete follow-up for one year
boolean
C0009488 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C3274571 (UMLS CUI [2,1])
C0205197 (UMLS CUI [2,2])
C0750558 (UMLS CUI [2,3])
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