ID

19538

Description

KONVERT-AF - Relevance of Point in Time for Conversion of Acute Atrial Fibrillation; ODM derived from: https://clinicaltrials.gov/show/NCT00369330

Lien

https://clinicaltrials.gov/show/NCT00369330

Mots-clés

Versions (2)
  1. 07/01/2017 07/01/2017 -
  2. 08/01/2017 08/01/2017 -
Téléchargé le

8 janvier 2017

DOI

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Licence

Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT00369330

Anglais

Eligibility Atrial Fibrillation NCT00369330

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
documented af that began between 2 and 8 hrs before randomization
Description

Atrial Fibrillation disease length

Type de données

boolean

Alias
UMLS CUI [1,1]
C0004238
UMLS CUI [1,2]
C0872146
indication for electrical cardioversion.
Description

Indication Electric Countershock

Type de données

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0013778
age above 18 yrs
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
written informed consent
Description

Informed Consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
af caused by not adequately treated reversible conditions(e.g. myocardial infarction, thyrotoxicosis, ethanol intoxication, infection, pericarditis, surgery)
Description

Medical condition Reversible Treated Inadequate | Atrial Fibrillation caused by Medical condition | Myocardial Infarction | Thyrotoxicosis | Toxic effect of ethyl alcohol | Communicable Disease | Pericarditis | Operative Surgical Procedures

Type de données

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C0205343
UMLS CUI [1,3]
C1522326
UMLS CUI [1,4]
C0205412
UMLS CUI [2,1]
C0004238
UMLS CUI [2,2]
C0015127
UMLS CUI [2,3]
C3843040
UMLS CUI [3]
C0027051
UMLS CUI [4]
C0040156
UMLS CUI [5]
C0161679
UMLS CUI [6]
C0009450
UMLS CUI [7]
C0031046
UMLS CUI [8]
C0543467
newly initiated (i.e. within 7 days before randomization) antiarrhythmic agents of class i, ii and/or iii
Description

Anti-Arrhythmia Agents Class

Type de données

boolean

Alias
UMLS CUI [1,1]
C0003195
UMLS CUI [1,2]
C2983595
catheter ablation of af within 3 months before randomization
Description

catheter ablation for atrial fibrillation

Type de données

boolean

Alias
UMLS CUI [1]
C2702800
pacemaker or icd
Description

Artificial cardiac pacemaker | Implantable defibrillator

Type de données

boolean

Alias
UMLS CUI [1]
C0030163
UMLS CUI [2]
C0162589
myocardial infarction within 3 months before randomization
Description

Myocardial Infarction

Type de données

boolean

Alias
UMLS CUI [1]
C0027051
urgent need to cardioversion of af because of associated potentially dangerous symptoms such as chest pain, syncope, dyspnea
Description

ATRIAL FIBRILLATION CARDIOVERSION Need Urgent | Dangerous symptoms Possibly | Chest Pain | Syncope | Dyspnea

Type de données

boolean

Alias
UMLS CUI [1,1]
C0741278
UMLS CUI [1,2]
C0686904
UMLS CUI [1,3]
C0439609
UMLS CUI [2,1]
C2164151
UMLS CUI [2,2]
C0332149
UMLS CUI [3]
C0008031
UMLS CUI [4]
C0039070
UMLS CUI [5]
C0013404
contraindications for therapy with vitamin k-antagonists
Description

Medical contraindication Treatment with Vitamin K antagonist

Type de données

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C1096489
intracardial thrombus
Description

Intracardiac thrombus

Type de données

boolean

Alias
UMLS CUI [1]
C0876998
primary indication for pharmacological cardioversion
Description

Indication Primary Pharmacological cardioversion

Type de données

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0205225
UMLS CUI [1,3]
C1963873
in females: pregnancy, lactation period or no sufficient contraception within last 3 months
Description

Gender | Pregnancy | Breast Feeding | Contraceptive methods Insufficient

Type de données

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0032961
UMLS CUI [3]
C0006147
UMLS CUI [4,1]
C0700589
UMLS CUI [4,2]
C0231180
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Similar models

Eligibility Atrial Fibrillation NCT00369330

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Atrial Fibrillation disease length
Item
documented af that began between 2 and 8 hrs before randomization
boolean
C0004238 (UMLS CUI [1,1])
C0872146 (UMLS CUI [1,2])
Indication Electric Countershock
Item
indication for electrical cardioversion.
boolean
C3146298 (UMLS CUI [1,1])
C0013778 (UMLS CUI [1,2])
Age
Item
age above 18 yrs
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Medical condition Reversible Treated Inadequate | Atrial Fibrillation caused by Medical condition | Myocardial Infarction | Thyrotoxicosis | Toxic effect of ethyl alcohol | Communicable Disease | Pericarditis | Operative Surgical Procedures
Item
af caused by not adequately treated reversible conditions(e.g. myocardial infarction, thyrotoxicosis, ethanol intoxication, infection, pericarditis, surgery)
boolean
C3843040 (UMLS CUI [1,1])
C0205343 (UMLS CUI [1,2])
C1522326 (UMLS CUI [1,3])
C0205412 (UMLS CUI [1,4])
C0004238 (UMLS CUI [2,1])
C0015127 (UMLS CUI [2,2])
C3843040 (UMLS CUI [2,3])
C0027051 (UMLS CUI [3])
C0040156 (UMLS CUI [4])
C0161679 (UMLS CUI [5])
C0009450 (UMLS CUI [6])
C0031046 (UMLS CUI [7])
C0543467 (UMLS CUI [8])
Anti-Arrhythmia Agents Class
Item
newly initiated (i.e. within 7 days before randomization) antiarrhythmic agents of class i, ii and/or iii
boolean
C0003195 (UMLS CUI [1,1])
C2983595 (UMLS CUI [1,2])
catheter ablation for atrial fibrillation
Item
catheter ablation of af within 3 months before randomization
boolean
C2702800 (UMLS CUI [1])
Artificial cardiac pacemaker | Implantable defibrillator
Item
pacemaker or icd
boolean
C0030163 (UMLS CUI [1])
C0162589 (UMLS CUI [2])
Myocardial Infarction
Item
myocardial infarction within 3 months before randomization
boolean
C0027051 (UMLS CUI [1])
ATRIAL FIBRILLATION CARDIOVERSION Need Urgent | Dangerous symptoms Possibly | Chest Pain | Syncope | Dyspnea
Item
urgent need to cardioversion of af because of associated potentially dangerous symptoms such as chest pain, syncope, dyspnea
boolean
C0741278 (UMLS CUI [1,1])
C0686904 (UMLS CUI [1,2])
C0439609 (UMLS CUI [1,3])
C2164151 (UMLS CUI [2,1])
C0332149 (UMLS CUI [2,2])
C0008031 (UMLS CUI [3])
C0039070 (UMLS CUI [4])
C0013404 (UMLS CUI [5])
Medical contraindication Treatment with Vitamin K antagonist
Item
contraindications for therapy with vitamin k-antagonists
boolean
C1301624 (UMLS CUI [1,1])
C1096489 (UMLS CUI [1,2])
Intracardiac thrombus
Item
intracardial thrombus
boolean
C0876998 (UMLS CUI [1])
Indication Primary Pharmacological cardioversion
Item
primary indication for pharmacological cardioversion
boolean
C3146298 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
C1963873 (UMLS CUI [1,3])
Gender | Pregnancy | Breast Feeding | Contraceptive methods Insufficient
Item
in females: pregnancy, lactation period or no sufficient contraception within last 3 months
boolean
C0079399 (UMLS CUI [1])
C0032961 (UMLS CUI [2])
C0006147 (UMLS CUI [3])
C0700589 (UMLS CUI [4,1])
C0231180 (UMLS CUI [4,2])
Retour au début de la page 

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