ID

4709

Description

Mots-clés

  1. 11/11/2011 11/11/2011 -
  2. 21/03/2014 21/03/2014 - Martin Dugas
Téléchargé le

21 mars 2014

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0 Legacy

Modèle Commentaires :

Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.

Groupe Item commentaires pour :

Item commentaires pour :

Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.

Eligibility Criteria NCT00035451 AF

Eligibility

  1. StudyEvent: Eligibility
    1. Eligibility
Inclusion criteria
Description

Inclusion criteria

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

History of atrial fibrillation

Type de données

boolean

Alias
UMLS CUI-1
C0004238
UMLS CUI-2
C1623258
procedure of cardioversion (electric shock to correct abnormal rhythm)
Description

Cardioversion

Type de données

boolean

Alias
UMLS CUI-1
C0013778
Patient anticoagulated according to the recommendations of the Study Group on Atrial Fibrillation of the European Society of Cardiology guidelines
Description

Anticoagulation

Type de données

boolean

Alias
UMLS CUI-1
C0449867
Exclusion criteria
Description

Exclusion criteria

Previously unsuccessful electrical cardioversions
Description

Previous cardioversions

Type de données

boolean

Alias
UMLS CUI-1
C0013778
Failed to respond to any Class III antiarrhythmic drugs
Description

Antiarrhythmic drugs

Type de données

boolean

Alias
UMLS CUI-1
C0003195
Qualifying arrhythmia due to acute reversible illness, acute myocardial infarction, and/or cardiac or thoracic surgery within one month prior to randomization
Description

Qualifying arrhythmia

Type de données

boolean

Alias
UMLS CUI-1
C0003811

Similar models

Eligibility

  1. StudyEvent: Eligibility
    1. Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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)

Utilisez ce formulaire pour les retours, les questions et les améliorations suggérées.

Les champs marqués d’un * sont obligatoires.

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