ID

43663

Descripción

Optimal Anticoagulation for Higher Risk Patients Post-Catheter Ablation for Atrial Fibrillation Trial; ODM derived from: https://clinicaltrials.gov/show/NCT02168829

Link

https://clinicaltrials.gov/show/NCT02168829

Palabras clave

Versiones (2)
  1. 25/4/16 25/4/16 -
  2. 20/9/21 20/9/21 -
Subido en

20 de septiembre de 2021

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT02168829

Inglés

Eligibility Atrial Fibrillation NCT02168829

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
at least one year post-successful catheter ablation for af or left atrial arrhythmia. successful af ablation is defined as no af/afl/at >30 seconds on any pre-enrolment monitoring
Descripción

Cardiac ablation Atrial Fibrillation | Cardiac ablation Left atrial structure Cardiac Arrhythmia | Atrial Flutter

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0162563
UMLS CUI [1,2]
C0004238
UMLS CUI [2,1]
C0162563
UMLS CUI [2,2]
C0225860
UMLS CUI [2,3]
C0003811
UMLS CUI [3]
C0004239
chads2 risk score of 1 or more. patients with chads2 score of 0, but who are >65 years old, or who are female with vascular disease will also be included
Descripción

Congestive heart failure, hypertension, age 75 years or older, diabetes, and previous stroke or transient ischemic attack risk score | Age | Female Vascular Diseases

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2585876
UMLS CUI [2]
C0001779
UMLS CUI [3,1]
C0086287
UMLS CUI [3,2]
C0042373
> 18 years of age
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
does not meet all of the above listed inclusion criteria.
Descripción

Negation Inclusion

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1518422
UMLS CUI [1,2]
C1512693
unable or unwilling to provide informed consent.
Descripción

Unable Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1299582
UMLS CUI [1,2]
C0021430
included in another clinical trial
Descripción

Study Subject Participation Status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
gfr < 30 ml/min
Descripción

Glomerular Filtration Rate

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0017654
contraindication to oral anticoagulation (oac)
Descripción

Medical contraindication Oral anticoagulants

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0354604
metallic prosthetic heart valve
Descripción

Metallic Heart Valve Prosthesis

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0018825
UMLS CUI [1,2]
C2986473
non-arrhythmic condition necessitating long-term oac
Descripción

Disease Requirement Long-term oral anticoagulants

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C1514873
UMLS CUI [1,3]
C0354604
UMLS CUI [1,4]
C0443252
stroke within one year prior to enrolment
Descripción

Cerebrovascular accident

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0038454
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Similar models

Eligibility Atrial Fibrillation NCT02168829

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Cardiac ablation Atrial Fibrillation | Cardiac ablation Left atrial structure Cardiac Arrhythmia | Atrial Flutter
Item
at least one year post-successful catheter ablation for af or left atrial arrhythmia. successful af ablation is defined as no af/afl/at >30 seconds on any pre-enrolment monitoring
boolean
C0162563 (UMLS CUI [1,1])
C0004238 (UMLS CUI [1,2])
C0162563 (UMLS CUI [2,1])
C0225860 (UMLS CUI [2,2])
C0003811 (UMLS CUI [2,3])
C0004239 (UMLS CUI [3])
Congestive heart failure, hypertension, age 75 years or older, diabetes, and previous stroke or transient ischemic attack risk score | Age | Female Vascular Diseases
Item
chads2 risk score of 1 or more. patients with chads2 score of 0, but who are >65 years old, or who are female with vascular disease will also be included
boolean
C2585876 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0086287 (UMLS CUI [3,1])
C0042373 (UMLS CUI [3,2])
Age
Item
> 18 years of age
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Negation Inclusion
Item
does not meet all of the above listed inclusion criteria.
boolean
C1518422 (UMLS CUI [1,1])
C1512693 (UMLS CUI [1,2])
Unable Informed Consent
Item
unable or unwilling to provide informed consent.
boolean
C1299582 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
Study Subject Participation Status
Item
included in another clinical trial
boolean
C2348568 (UMLS CUI [1])
Glomerular Filtration Rate
Item
gfr < 30 ml/min
boolean
C0017654 (UMLS CUI [1])
Medical contraindication Oral anticoagulants
Item
contraindication to oral anticoagulation (oac)
boolean
C1301624 (UMLS CUI [1,1])
C0354604 (UMLS CUI [1,2])
Metallic Heart Valve Prosthesis
Item
metallic prosthetic heart valve
boolean
C0018825 (UMLS CUI [1,1])
C2986473 (UMLS CUI [1,2])
Disease Requirement Long-term oral anticoagulants
Item
non-arrhythmic condition necessitating long-term oac
boolean
C0012634 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0354604 (UMLS CUI [1,3])
C0443252 (UMLS CUI [1,4])
Cerebrovascular accident
Item
stroke within one year prior to enrolment
boolean
C0038454 (UMLS CUI [1])
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