ID

34576

Beschrijving

Non-interventional Local Study on Prescription Behavior of Anticoagulation Therapy in Secondary Stroke Prevention in Atrial Fibrillation Patients; ODM derived from: https://clinicaltrials.gov/show/NCT01925755

Link

https://clinicaltrials.gov/show/NCT01925755

Trefwoorden

  1. 19-01-19 19-01-19 -
  2. 28-09-20 28-09-20 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

19 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

Model Commentaren :

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Eligibility Stroke, NCT01925755

Eligibility Stroke, NCT01925755

  1. StudyEvent: Eligibility
    1. Eligibility Stroke, NCT01925755
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
male and female patients ≥ 18 years old who start treatment with rivaroxaban
Beschrijving

ID.1

Datatype

boolean

non-valvular atrial fibrillation is documented in patients' file
Beschrijving

ID.2

Datatype

boolean

prior tia/stroke history
Beschrijving

ID.3

Datatype

boolean

tia - more than 72 hours after documented tia
Beschrijving

ID.4

Datatype

boolean

more than 2 weeks after non-hemorrhagic stroke
Beschrijving

ID.5

Datatype

boolean

written informed consent
Beschrijving

ID.6

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
contraindications for use of xarelto® in accordance with approved product label
Beschrijving

ID.7

Datatype

boolean

previous thromboprophylaxis treatment with anticoagulants prior toby reason of stroke
Beschrijving

ID.8

Datatype

boolean

/ tia prevention
Beschrijving

ID.9

Datatype

boolean

any reasons of medical and non-medical character, which in the opinion of the physician can hamper patient participation in nis
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Stroke, NCT01925755

  1. StudyEvent: Eligibility
    1. Eligibility Stroke, NCT01925755
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
male and female patients ≥ 18 years old who start treatment with rivaroxaban
boolean
ID.2
Item
non-valvular atrial fibrillation is documented in patients' file
boolean
ID.3
Item
prior tia/stroke history
boolean
ID.4
Item
tia - more than 72 hours after documented tia
boolean
ID.5
Item
more than 2 weeks after non-hemorrhagic stroke
boolean
ID.6
Item
written informed consent
boolean
Item Group
C0680251 (UMLS CUI)
ID.7
Item
contraindications for use of xarelto® in accordance with approved product label
boolean
ID.8
Item
previous thromboprophylaxis treatment with anticoagulants prior toby reason of stroke
boolean
ID.9
Item
/ tia prevention
boolean
ID.10
Item
any reasons of medical and non-medical character, which in the opinion of the physician can hamper patient participation in nis
boolean

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