Informations:
Erreur:
ID
20399
Description
n-3 Polyunsaturated Fatty Acids (PUFAs) in the Prevention of Atrial Fibrillation; ODM derived from: https://clinicaltrials.gov/show/NCT01198275
Lien
https://clinicaltrials.gov/show/NCT01198275
Mots-clés
Versions (1)
- 21/02/2017 21/02/2017 -
Téléchargé le
21 février 2017
DOI
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Licence
Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT01198275
Eligibility Atrial Fibrillation NCT01198275
- StudyEvent: Eligibility
Similar models
Eligibility Atrial Fibrillation NCT01198275
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
persistent atrial fibrillation
Item
persistent atrial fibrillation (af) lasting > one month
boolean
C2585653 (UMLS CUI [1])
atrial fibrillation | Medical History, Relapse | Pharmacological cardioversion | Electric Countershock
Item
history of at least one af relapse after previous electrical or pharmacological cardioversion
boolean
C0004238 (UMLS CUI [1])
C0262926 (UMLS CUI [2,1])
C0035020 (UMLS CUI [2,2])
C1963873 (UMLS CUI [3])
C0013778 (UMLS CUI [4])
C0262926 (UMLS CUI [2,1])
C0035020 (UMLS CUI [2,2])
C1963873 (UMLS CUI [3])
C0013778 (UMLS CUI [4])
left atrium size
Item
left atrium size > 6 cm
boolean
C1302212 (UMLS CUI [1])
severe valvulopathy
Item
severe valvulopathy
boolean
C0018824 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,2])
history of myocardial infarction
Item
myocardial infarction during the previous 6 months
boolean
C1275835 (UMLS CUI [1])
unstable angina
Item
unstable angina
boolean
C0002965 (UMLS CUI [1])
congestive heart failure, hemodynamic instability
Item
nyha heart failure class iv or hemodynamic instability
boolean
C0018802 (UMLS CUI [1,1])
C1319796 (UMLS CUI [1,2])
C0948268 (UMLS CUI [2])
C1319796 (UMLS CUI [1,2])
C0948268 (UMLS CUI [2])
cardiac surgery
Item
cardiac surgery during the previous 3 months
boolean
C0018821 (UMLS CUI [1])
pulmonary thyroid and hepatic disease
Item
significant pulmonary thyroid and hepatic disease
boolean
C0024115 (UMLS CUI [1])
C0023895 (UMLS CUI [2])
C0040128 (UMLS CUI [3])
C0023895 (UMLS CUI [2])
C0040128 (UMLS CUI [3])
contraindication to treatment with amiodarone or rass inhibitors
Item
contraindications to treatment with amiodarone or rass inhibitors
boolean
C1301624 (UMLS CUI [1,1])
C0002598 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C3653735 (UMLS CUI [2,2])
C0002598 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C3653735 (UMLS CUI [2,2])
chronic renal dysfunction
Item
chronic renal dysfunction
boolean
C0022661 (UMLS CUI [1])
Mean QT Duration | Bundle-Branch Block
Item
qt > 480 msec in the absence of bundle-branch block
boolean
C1880452 (UMLS CUI [1])
C0006384 (UMLS CUI [2])
C0006384 (UMLS CUI [2])
bradycardia
Item
bradycardia < 50 b/min
boolean
C0428977 (UMLS CUI [1])
paroxysmal atrial fibrillation
Item
diagnosis of paroxysmal af
boolean
C0235480 (UMLS CUI [1])
potassium measurement
Item
hyperkalemia
boolean
C0202194 (UMLS CUI [1])
pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Comorbidity; Limited (extensiveness); Study Protocol
Item
any disease or other medical treatment that, in the opinion of the investigators, could interfere with the study.
boolean
C0009488 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C2348563 (UMLS CUI [1,3])
C0439801 (UMLS CUI [1,2])
C2348563 (UMLS CUI [1,3])