ID

28372

Description

Investigator-initiated prospective randomized multicentre study to uncover the true burden of paroxysmal atrial fibrillation in a representative population of acute stroke patients without known atrial fibrillation. https://clinicaltrials.gov/ct2/show/NCT02204267?term=NCT02204267&rank=1. Sponsor: Charite University, Berlin, Germany; Collaborator: Bayer Healthcare Pharmaceuticals, Inc./Bayer Schering Pharma; Information provided by (Responsible Party): Matthias Endres, Charite University, Berlin, Germany

Link

https://clinicaltrials.gov/ct2/show/NCT02204267?term=NCT02204267&rank=1

Keywords

Versions (1)
  1. 1/8/18 1/8/18 -
Copyright Holder

Charite University, Berlin, Germany

Uploaded on

January 8, 2018

DOI

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License

Creative Commons BY-NC 3.0
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Eligibility Criteria MonDAFIS Atrial Fibrillation in Ischemic Stroke NCT02204267

English

Eligibility Criteria MonDAFIS Atrial Fibrillation in Ischemic Stroke NCT02204267

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Acute ischemic stroke or transitory ischemic attack (with clinical deficit on enrolment or MRI detected acute brain lesion on admission)
Description

Acute ischemic stroke or transitory ischemic attack

Data type

boolean

Age ≥ 18 years
Description

Age

Data type

boolean

Written or oral informed consent
Description

informed consent

Data type

boolean

Stroke unit admission within 72 hours after stroke onset
Description

Stroke unit admission

Data type

boolean

Start of standardized prolonged ECG monitoring within 24 hours after admission to the stroke unit
Description

ECG monitoring

Data type

boolean

Willingness to take part in the planned follow up examinations
Description

follow up examinations

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

Known atrial fibrillation
Description

Known atrial fibrillation

Data type

boolean

Atrial fibrillation detected by ECG on admission
Description

Atrial fibrillation detected admission

Data type

boolean

Atrial fibrillation detected prior study enrollment on the stroke unit
Description

Atrial fibrillation detected prior study enrollment

Data type

boolean

Life expectancy < 1 year (before actual stroke)
Description

Life expectancy less than 1 year

Data type

boolean

Life expectancy < 1 month (after actual stroke)
Description

Life expectancy less than 1 month

Data type

boolean

Indication for oral anticoagulation other than atrial fibrillation (e.g. mechanical heart valve)
Description

Indication for oral anticoagulation

Data type

boolean

Severity level according National Institute of Health Stroke Scale (NIHSS) score > 22
Description

NIHSS score

Data type

boolean

Participation in an interventional trial
Description

interventional trial

Data type

boolean

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Similar models

Eligibility Criteria MonDAFIS Atrial Fibrillation in Ischemic Stroke NCT02204267

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Inclusion Criteria
Acute ischemic stroke or transitory ischemic attack
Item
Acute ischemic stroke or transitory ischemic attack (with clinical deficit on enrolment or MRI detected acute brain lesion on admission)
boolean
Age
Item
Age ≥ 18 years
boolean
informed consent
Item
Written or oral informed consent
boolean
Stroke unit admission
Item
Stroke unit admission within 72 hours after stroke onset
boolean
ECG monitoring
Item
Start of standardized prolonged ECG monitoring within 24 hours after admission to the stroke unit
boolean
follow up examinations
Item
Willingness to take part in the planned follow up examinations
boolean
Item Group
Exclusion Criteria
Known atrial fibrillation
Item
Known atrial fibrillation
boolean
Atrial fibrillation detected admission
Item
Atrial fibrillation detected by ECG on admission
boolean
Atrial fibrillation detected prior study enrollment
Item
Atrial fibrillation detected prior study enrollment on the stroke unit
boolean
Life expectancy less than 1 year
Item
Life expectancy < 1 year (before actual stroke)
boolean
Life expectancy less than 1 month
Item
Life expectancy < 1 month (after actual stroke)
boolean
Indication for oral anticoagulation
Item
Indication for oral anticoagulation other than atrial fibrillation (e.g. mechanical heart valve)
boolean
NIHSS score
Item
Severity level according National Institute of Health Stroke Scale (NIHSS) score > 22
boolean
interventional trial
Item
Participation in an interventional trial
boolean
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