ID

19370

Descripción

Arrhythmia Restart Prevention and RatE STabilization in Atrial Fibrillation; ODM derived from: https://clinicaltrials.gov/show/NCT00224341

Link

https://clinicaltrials.gov/show/NCT00224341

Palabras clave

Versiones (1)
  1. 22/12/16 22/12/16 -
Subido en

22 de diciembre de 2016

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Sick Sinus Syndrome NCT00224341

Inglés

Eligibility Sick Sinus Syndrome NCT00224341

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
patient with documented atrial fibrillation: at least one episode of paroxysmal af documented 6 months prior to inclusion, lasting more than one minute
Descripción

Atrial Fibrillation | Paroxysmal atrial fibrillation Episode Quantity

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0004238
UMLS CUI [2,1]
C0235480
UMLS CUI [2,2]
C0332189
UMLS CUI [2,3]
C1265611
patient with a brady-tachy syndrome or a sick sinus syndrome, with a permanent pacing indication
Descripción

Bradycardia-tachycardia syndrome | Sick Sinus Syndrome | Indication Cardiac pacing Permanent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0221047
UMLS CUI [2]
C0037052
UMLS CUI [3,1]
C3146298
UMLS CUI [3,2]
C0199640
UMLS CUI [3,3]
C0205355
atrial lead with a tip-to-ring interval equal to or less than 12 mm
Descripción

Atrial Lead

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2825198
patient who agrees with and has signed the informed consent
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
permanent af
Descripción

Permanent atrial fibrillation

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2586056
af related to a reversible cause
Descripción

Atrial Fibrillation Due to Cause Reversible

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0004238
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C0015127
UMLS CUI [1,4]
C0205343
one electrical cardioversion 6 months prior to inclusion
Descripción

Electric Countershock Quantity

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0013778
UMLS CUI [1,2]
C1265611
unstable angina
Descripción

Angina, Unstable

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0002965
myocardial infarction (mi) less than 3 months
Descripción

Myocardial Infarction

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0027051
planned cardiac surgery or performed in the last 3 months
Descripción

Cardiac Surgery | Cardiac Surgery Planned

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0018821
UMLS CUI [2,1]
C0018821
UMLS CUI [2,2]
C1301732
congestive heart failure, new york heart association (nyha) class iv
Descripción

Congestive heart failure New York Heart Association Classification

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0018802
UMLS CUI [1,2]
C1275491
life expectancy less than 18 months
Descripción

Life Expectancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0023671
patient participating in other studies
Descripción

Study Subject Participation Status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
patient not able to follow the fu calendar
Descripción

Follow-up Compliance behavior Unable

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3274571
UMLS CUI [1,2]
C1321605
UMLS CUI [1,3]
C1299582
less than 18 years of age
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
pregnancy
Descripción

Pregnancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
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Similar models

Eligibility Sick Sinus Syndrome NCT00224341

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
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])
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])
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])
Item Group
C0680251 (UMLS CUI)
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])
Electric Countershock Quantity
Item
one electrical cardioversion 6 months prior to inclusion
boolean
C0013778 (UMLS CUI [1,1])
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])
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])
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])
Age
Item
less than 18 years of age
boolean
C0001779 (UMLS CUI [1])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
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