ID

28372

Beschrijving

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

Trefwoorden

Versies (1)
  1. 08-01-18 08-01-18 -
Houder van rechten

Charite University, Berlin, Germany

Geüploaded op

8 januari 2018

DOI

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Licentie

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

Engels

Eligibility Criteria MonDAFIS Atrial Fibrillation in Ischemic Stroke NCT02204267

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

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

Acute ischemic stroke or transitory ischemic attack

Datatype

boolean

Age ≥ 18 years
Beschrijving

Age

Datatype

boolean

Written or oral informed consent
Beschrijving

informed consent

Datatype

boolean

Stroke unit admission within 72 hours after stroke onset
Beschrijving

Stroke unit admission

Datatype

boolean

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

ECG monitoring

Datatype

boolean

Willingness to take part in the planned follow up examinations
Beschrijving

follow up examinations

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Known atrial fibrillation
Beschrijving

Known atrial fibrillation

Datatype

boolean

Atrial fibrillation detected by ECG on admission
Beschrijving

Atrial fibrillation detected admission

Datatype

boolean

Atrial fibrillation detected prior study enrollment on the stroke unit
Beschrijving

Atrial fibrillation detected prior study enrollment

Datatype

boolean

Life expectancy < 1 year (before actual stroke)
Beschrijving

Life expectancy less than 1 year

Datatype

boolean

Life expectancy < 1 month (after actual stroke)
Beschrijving

Life expectancy less than 1 month

Datatype

boolean

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

Indication for oral anticoagulation

Datatype

boolean

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

NIHSS score

Datatype

boolean

Participation in an interventional trial
Beschrijving

interventional trial

Datatype

boolean

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Similar models

Eligibility Criteria MonDAFIS Atrial Fibrillation in Ischemic Stroke NCT02204267

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
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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