Information:
Error:
ID
19370
Description
Arrhythmia Restart Prevention and RatE STabilization in Atrial Fibrillation; ODM derived from: https://clinicaltrials.gov/show/NCT00224341
Link
https://clinicaltrials.gov/show/NCT00224341
Keywords
Versions (1)
- 12/22/16 12/22/16 -
Uploaded on
December 22, 2016
DOI
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License
Creative Commons BY 4.0
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Eligibility Sick Sinus Syndrome NCT00224341
Eligibility Sick Sinus Syndrome NCT00224341
- StudyEvent: Eligibility
Similar models
Eligibility Sick Sinus Syndrome NCT00224341
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Atrial Fibrillation | Paroxysmal atrial fibrillation Episode Quantity
Item
patient with documented atrial fibrillation: at least one episode of paroxysmal af documented 6 months prior to inclusion, lasting more than one minute
boolean
C0004238 (UMLS CUI [1])
C0235480 (UMLS CUI [2,1])
C0332189 (UMLS CUI [2,2])
C1265611 (UMLS CUI [2,3])
C0235480 (UMLS CUI [2,1])
C0332189 (UMLS CUI [2,2])
C1265611 (UMLS CUI [2,3])
Bradycardia-tachycardia syndrome | Sick Sinus Syndrome | Indication Cardiac pacing Permanent
Item
patient with a brady-tachy syndrome or a sick sinus syndrome, with a permanent pacing indication
boolean
C0221047 (UMLS CUI [1])
C0037052 (UMLS CUI [2])
C3146298 (UMLS CUI [3,1])
C0199640 (UMLS CUI [3,2])
C0205355 (UMLS CUI [3,3])
C0037052 (UMLS CUI [2])
C3146298 (UMLS CUI [3,1])
C0199640 (UMLS CUI [3,2])
C0205355 (UMLS CUI [3,3])
Atrial Lead
Item
atrial lead with a tip-to-ring interval equal to or less than 12 mm
boolean
C2825198 (UMLS CUI [1])
Informed Consent
Item
patient who agrees with and has signed the informed consent
boolean
C0021430 (UMLS CUI [1])
Permanent atrial fibrillation
Item
permanent af
boolean
C2586056 (UMLS CUI [1])
Atrial Fibrillation Due to Cause Reversible
Item
af related to a reversible cause
boolean
C0004238 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C0015127 (UMLS CUI [1,3])
C0205343 (UMLS CUI [1,4])
C0678226 (UMLS CUI [1,2])
C0015127 (UMLS CUI [1,3])
C0205343 (UMLS CUI [1,4])
Electric Countershock Quantity
Item
one electrical cardioversion 6 months prior to inclusion
boolean
C0013778 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,2])
Angina, Unstable
Item
unstable angina
boolean
C0002965 (UMLS CUI [1])
Myocardial Infarction
Item
myocardial infarction (mi) less than 3 months
boolean
C0027051 (UMLS CUI [1])
Cardiac Surgery | Cardiac Surgery Planned
Item
planned cardiac surgery or performed in the last 3 months
boolean
C0018821 (UMLS CUI [1])
C0018821 (UMLS CUI [2,1])
C1301732 (UMLS CUI [2,2])
C0018821 (UMLS CUI [2,1])
C1301732 (UMLS CUI [2,2])
Congestive heart failure New York Heart Association Classification
Item
congestive heart failure, new york heart association (nyha) class iv
boolean
C0018802 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
C1275491 (UMLS CUI [1,2])
Life Expectancy
Item
life expectancy less than 18 months
boolean
C0023671 (UMLS CUI [1])
Study Subject Participation Status
Item
patient participating in other studies
boolean
C2348568 (UMLS CUI [1])
Follow-up Compliance behavior Unable
Item
patient not able to follow the fu calendar
boolean
C3274571 (UMLS CUI [1,1])
C1321605 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
C1321605 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
Age
Item
less than 18 years of age
boolean
C0001779 (UMLS CUI [1])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])