ID

4709

Beschrijving

Trefwoorden

  1. 11-11-11 11-11-11 -
  2. 21-03-14 21-03-14 - Martin Dugas
Geüploaded op

21 maart 2014

DOI

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Licentie

Creative Commons BY-NC 3.0 Legacy

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Eligibility Criteria NCT00035451 AF

Eligibility

  1. StudyEvent: Eligibility
    1. Eligibility
Inclusion criteria
Beschrijving

Inclusion criteria

Documented (12-lead ECG) history of symptomatic atrial fibrillation occurring between 48 hours and 6 months before screening
Beschrijving

History of atrial fibrillation

Datatype

boolean

Alias
UMLS CUI-1
C0004238 (Atrial Fibrillation)
SNOMED
49436004
UMLS CUI-2
C1623258 (Electrocardiography)
SNOMED
29303009
LOINC
LP6244-0
procedure of cardioversion (electric shock to correct abnormal rhythm)
Beschrijving

Cardioversion

Datatype

boolean

Alias
UMLS CUI-1
C0013778 (Electric Countershock)
SNOMED
250980009
LOINC
LP97905-1
Patient anticoagulated according to the recommendations of the Study Group on Atrial Fibrillation of the European Society of Cardiology guidelines
Beschrijving

Anticoagulation

Datatype

boolean

Alias
UMLS CUI-1
C0449867 (Use of anticoagulation)
SNOMED
260678004
Exclusion criteria
Beschrijving

Exclusion criteria

Previously unsuccessful electrical cardioversions
Beschrijving

Previous cardioversions

Datatype

boolean

Alias
UMLS CUI-1
C0013778 (Electric Countershock)
SNOMED
250980009
LOINC
LP97905-1
Failed to respond to any Class III antiarrhythmic drugs
Beschrijving

Antiarrhythmic drugs

Datatype

boolean

Alias
UMLS CUI-1
C0003195 (Anti-Arrhythmia Agents)
SNOMED
67507000
Qualifying arrhythmia due to acute reversible illness, acute myocardial infarction, and/or cardiac or thoracic surgery within one month prior to randomization
Beschrijving

Qualifying arrhythmia

Datatype

boolean

Alias
UMLS CUI-1
C0003811 (Cardiac Arrhythmia)
SNOMED
698247007
LOINC
LA7414-1

Similar models

Eligibility

  1. StudyEvent: Eligibility
    1. Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Inclusion criteria
History of atrial fibrillation
Item
Documented (12-lead ECG) history of symptomatic atrial fibrillation occurring between 48 hours and 6 months before screening
boolean
C0004238 (UMLS CUI-1)
C1623258 (UMLS CUI-2)
Cardioversion
Item
procedure of cardioversion (electric shock to correct abnormal rhythm)
boolean
C0013778 (UMLS CUI-1)
Anticoagulation
Item
Patient anticoagulated according to the recommendations of the Study Group on Atrial Fibrillation of the European Society of Cardiology guidelines
boolean
C0449867 (UMLS CUI-1)
Item Group
Exclusion criteria
Previous cardioversions
Item
Previously unsuccessful electrical cardioversions
boolean
C0013778 (UMLS CUI-1)
Antiarrhythmic drugs
Item
Failed to respond to any Class III antiarrhythmic drugs
boolean
C0003195 (UMLS CUI-1)
Qualifying arrhythmia
Item
Qualifying arrhythmia due to acute reversible illness, acute myocardial infarction, and/or cardiac or thoracic surgery within one month prior to randomization
boolean
C0003811 (UMLS CUI-1)

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