ID

28372

Descripción

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

Palabras clave

  1. 8/1/18 8/1/18 -
Titular de derechos de autor

Charite University, Berlin, Germany

Subido en

8 de enero de 2018

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY-NC 3.0

Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Comentarios de grupo de elementos para :

Comentarios del elemento para :

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

Eligibility Criteria MonDAFIS Atrial Fibrillation in Ischemic Stroke NCT02204267

Eligibility Criteria MonDAFIS Atrial Fibrillation in Ischemic Stroke NCT02204267

Inclusion Criteria
Descripción

Inclusion Criteria

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

Acute ischemic stroke or transitory ischemic attack

Tipo de datos

boolean

Age ≥ 18 years
Descripción

Age

Tipo de datos

boolean

Written or oral informed consent
Descripción

informed consent

Tipo de datos

boolean

Stroke unit admission within 72 hours after stroke onset
Descripción

Stroke unit admission

Tipo de datos

boolean

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

ECG monitoring

Tipo de datos

boolean

Willingness to take part in the planned follow up examinations
Descripción

follow up examinations

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

Known atrial fibrillation
Descripción

Known atrial fibrillation

Tipo de datos

boolean

Atrial fibrillation detected by ECG on admission
Descripción

Atrial fibrillation detected admission

Tipo de datos

boolean

Atrial fibrillation detected prior study enrollment on the stroke unit
Descripción

Atrial fibrillation detected prior study enrollment

Tipo de datos

boolean

Life expectancy < 1 year (before actual stroke)
Descripción

Life expectancy less than 1 year

Tipo de datos

boolean

Life expectancy < 1 month (after actual stroke)
Descripción

Life expectancy less than 1 month

Tipo de datos

boolean

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

Indication for oral anticoagulation

Tipo de datos

boolean

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

NIHSS score

Tipo de datos

boolean

Participation in an interventional trial
Descripción

interventional trial

Tipo de datos

boolean

Similar models

Eligibility Criteria MonDAFIS Atrial Fibrillation in Ischemic Stroke NCT02204267

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial