0 Ratings

ID

43663

Description

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

Keywords

  1. 4/25/16 4/25/16 -
  2. 9/20/21 9/20/21 -
Uploaded on

September 20, 2021

DOI

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License

Creative Commons BY 4.0

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    Eligibility Atrial Fibrillation NCT02168829

    Eligibility Atrial Fibrillation NCT02168829

    Inclusion Criteria
    Description

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693 (Inclusion)
    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
    Description

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

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0162563 (Cardiac ablation)
    UMLS CUI [1,2]
    C0004238 (Atrial Fibrillation)
    SNOMED
    49436004
    UMLS CUI [2,1]
    C0162563 (Cardiac ablation)
    UMLS CUI [2,2]
    C0225860 (Left atrial structure)
    SNOMED
    264069002
    UMLS CUI [2,3]
    C0003811 (Cardiac Arrhythmia)
    SNOMED
    698247007
    LOINC
    LA7414-1
    UMLS CUI [3]
    C0004239 (Atrial Flutter)
    SNOMED
    5370000
    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
    Description

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

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C2585876 (CHADS2 score)
    SNOMED
    438367009
    UMLS CUI [2]
    C0001779 (Age)
    SNOMED
    424144002
    LOINC
    LP28815-6
    UMLS CUI [3,1]
    C0086287 (Females)
    SNOMED
    1086007
    UMLS CUI [3,2]
    C0042373 (Vascular Diseases)
    SNOMED
    27550009
    > 18 years of age
    Description

    Age

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0001779 (Age)
    SNOMED
    424144002
    LOINC
    LP28815-6
    Exclusion Criteria
    Description

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251 (Exclusion Criteria)
    does not meet all of the above listed inclusion criteria.
    Description

    Negation Inclusion

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C1518422 (Negation)
    LOINC
    LA21291-2
    UMLS CUI [1,2]
    C1512693 (Inclusion)
    unable or unwilling to provide informed consent.
    Description

    Unable Informed Consent

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C1299582 (Unable)
    SNOMED
    371151008
    LOINC
    LA13868-7
    UMLS CUI [1,2]
    C0021430 (Informed Consent)
    included in another clinical trial
    Description

    Study Subject Participation Status

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C2348568 (Study Subject Participation Status)
    gfr < 30 ml/min
    Description

    Glomerular Filtration Rate

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0017654 (Glomerular Filtration Rate)
    SNOMED
    80274001
    contraindication to oral anticoagulation (oac)
    Description

    Medical contraindication Oral anticoagulants

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C1301624 (Medical contraindication)
    SNOMED
    397745006
    LOINC
    LA27164-5
    UMLS CUI [1,2]
    C0354604 (oral anticoagulants)
    metallic prosthetic heart valve
    Description

    Metallic Heart Valve Prosthesis

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0018825 (Heart Valve Prosthesis)
    SNOMED
    25510005
    UMLS CUI [1,2]
    C2986473 (Metallic)
    non-arrhythmic condition necessitating long-term oac
    Description

    Disease Requirement Long-term oral anticoagulants

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0012634 (Disease)
    SNOMED
    64572001
    LOINC
    LP21006-9
    UMLS CUI [1,2]
    C1514873 (Requirement)
    UMLS CUI [1,3]
    C0354604 (oral anticoagulants)
    UMLS CUI [1,4]
    C0443252 (Long-term)
    stroke within one year prior to enrolment
    Description

    Cerebrovascular accident

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0038454 (Cerebrovascular accident)
    SNOMED
    230690007
    LOINC
    MTHU020801

    Similar models

    Eligibility Atrial Fibrillation NCT02168829

    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    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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