0 Ratings
ID

40480

Description

Detecting Heart Disease Using First Pass Imaging With Gated SPECT Perfusion; ODM derived from: https://clinicaltrials.gov/show/NCT01137409

Link

https://clinicaltrials.gov/show/NCT01137409

Keywords

Versions (1)
  1. 4/25/20 4/25/20 -
Copyright Holder

See clinicaltrials.gov

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April 25, 2020

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License

Creative Commons BY 4.0
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    Eligibility Ischemic Heart Disease NCT01137409

    English

    Eligibility Ischemic Heart Disease NCT01137409

    1 forms  
    Inclusion Criteria
    Description

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    males and females age 18 through 80 years
    Description

    Age

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    female patients who are: surgically sterile (hysterectomy or bilateral tubule libation), at least one year post-menopausal, or have a negative pregnancy test on the day of treatment
    Description

    Gender | Female Sterilization | Hysterectomy | Bilateral tubal ligation | Postmenopausal state Duration | Pregnancy test negative

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0079399
    UMLS CUI [2]
    C0015787
    UMLS CUI [3]
    C0020699
    UMLS CUI [4]
    C0589114
    UMLS CUI [5,1]
    C0232970
    UMLS CUI [5,2]
    C0449238
    UMLS CUI [6]
    C0427780
    written informed consent
    Description

    Informed Consent

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0021430
    Exclusion Criteria
    Description

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    patient consumed food/beverage/medication containing caffeine/methylxanthines up to 12 hours prior to infusion
    Description

    Food Containing Caffeine | Beverages Containing Caffeine | Pharmaceutical Preparations Containing Caffeine | Food Containing Methylxanthine | Beverages Containing Methylxanthine | Pharmaceutical Preparations Containing Methylxanthine

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0016452
    UMLS CUI [1,2]
    C0332256
    UMLS CUI [1,3]
    C0006644
    UMLS CUI [2,1]
    C0005329
    UMLS CUI [2,2]
    C0332256
    UMLS CUI [2,3]
    C0006644
    UMLS CUI [3,1]
    C0013227
    UMLS CUI [3,2]
    C0332256
    UMLS CUI [3,3]
    C0006644
    UMLS CUI [4,1]
    C0016452
    UMLS CUI [4,2]
    C0332256
    UMLS CUI [4,3]
    C0066447
    UMLS CUI [5,1]
    C0005329
    UMLS CUI [5,2]
    C0332256
    UMLS CUI [5,3]
    C0066447
    UMLS CUI [6,1]
    C0013227
    UMLS CUI [6,2]
    C0332256
    UMLS CUI [6,3]
    C0066447
    exacerbation of copd, asthma (actively wheezing)
    Description

    COPD exacerbation | Asthma | Wheezing

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0740304
    UMLS CUI [2]
    C0004096
    UMLS CUI [3]
    C0043144
    sinus node dysfunction in absence of pacemaker
    Description

    Sinus Node Dysfunction | Artificial cardiac pacemaker Absent

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0428908
    UMLS CUI [2,1]
    C0030163
    UMLS CUI [2,2]
    C0332197
    use of aggrenox (asa/dipyridamole), pentoxifylline (trental) , or oral dipyridamole (persantine)
    Description

    Aggrenox | Aspirin | Dipyridamole | Pentoxifylline | Trental | Dipyridamole Oral [Persantine]

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0732282
    UMLS CUI [2]
    C0004057
    UMLS CUI [3]
    C0012582
    UMLS CUI [4]
    C0030899
    UMLS CUI [5]
    C0699487
    UMLS CUI [6]
    C1242076
    atrial fibrillation
    Description

    Atrial Fibrillation

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0004238
    pregnant/breast feeding
    Description

    Pregnancy | Breast Feeding

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0032961
    UMLS CUI [2]
    C0006147
    non english speaking patients
    Description

    Lacking Able to speak English Language

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0332268
    UMLS CUI [1,2]
    C0564215
    UMLS CUI [1,3]
    C0376245
    subject is allergic or intolerant to aminophylline, regadenoson
    Description

    Aminophylline allergy | Intolerance to Aminophylline | Hypersensitivity Regadenoson | Intolerance to Regadenoson

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0571074
    UMLS CUI [2,1]
    C1744706
    UMLS CUI [2,2]
    C0002575
    UMLS CUI [3,1]
    C0020517
    UMLS CUI [3,2]
    C1698215
    UMLS CUI [4,1]
    C1744706
    UMLS CUI [4,2]
    C1698215
    subject has a history of known or suspected bronchospastic lung disease [e.g., asthma, wheezing, chronic obstructive pulmonary disease (copd, etc.)]
    Description

    Lung disease Bronchial Spasm | Bronchial Spasm Suspected | Asthma | Wheezing | Chronic Obstructive Airway Disease

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0024115
    UMLS CUI [1,2]
    C0006266
    UMLS CUI [2,1]
    C0006266
    UMLS CUI [2,2]
    C0750491
    UMLS CUI [3]
    C0004096
    UMLS CUI [4]
    C0043144
    UMLS CUI [5]
    C0024117
    patients with first degree or second degree av block
    Description

    First degree atrioventricular block | Second degree atrioventricular block

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0085614
    UMLS CUI [2]
    C0264906
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    Similar models

    Eligibility Ischemic Heart Disease NCT01137409

    1 forms
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    C1512693 (UMLS CUI)
    Age
    Item
    males and females age 18 through 80 years
    boolean
    C0001779 (UMLS CUI [1])
    Gender | Female Sterilization | Hysterectomy | Bilateral tubal ligation | Postmenopausal state Duration | Pregnancy test negative
    Item
    female patients who are: surgically sterile (hysterectomy or bilateral tubule libation), at least one year post-menopausal, or have a negative pregnancy test on the day of treatment
    boolean
    C0079399 (UMLS CUI [1])
    C0015787 (UMLS CUI [2])
    C0020699 (UMLS CUI [3])
    C0589114 (UMLS CUI [4])
    C0232970 (UMLS CUI [5,1])
    C0449238 (UMLS CUI [5,2])
    C0427780 (UMLS CUI [6])
    Informed Consent
    Item
    written informed consent
    boolean
    C0021430 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    Food Containing Caffeine | Beverages Containing Caffeine | Pharmaceutical Preparations Containing Caffeine | Food Containing Methylxanthine | Beverages Containing Methylxanthine | Pharmaceutical Preparations Containing Methylxanthine
    Item
    patient consumed food/beverage/medication containing caffeine/methylxanthines up to 12 hours prior to infusion
    boolean
    C0016452 (UMLS CUI [1,1])
    C0332256 (UMLS CUI [1,2])
    C0006644 (UMLS CUI [1,3])
    C0005329 (UMLS CUI [2,1])
    C0332256 (UMLS CUI [2,2])
    C0006644 (UMLS CUI [2,3])
    C0013227 (UMLS CUI [3,1])
    C0332256 (UMLS CUI [3,2])
    C0006644 (UMLS CUI [3,3])
    C0016452 (UMLS CUI [4,1])
    C0332256 (UMLS CUI [4,2])
    C0066447 (UMLS CUI [4,3])
    C0005329 (UMLS CUI [5,1])
    C0332256 (UMLS CUI [5,2])
    C0066447 (UMLS CUI [5,3])
    C0013227 (UMLS CUI [6,1])
    C0332256 (UMLS CUI [6,2])
    C0066447 (UMLS CUI [6,3])
    COPD exacerbation | Asthma | Wheezing
    Item
    exacerbation of copd, asthma (actively wheezing)
    boolean
    C0740304 (UMLS CUI [1])
    C0004096 (UMLS CUI [2])
    C0043144 (UMLS CUI [3])
    Sinus Node Dysfunction | Artificial cardiac pacemaker Absent
    Item
    sinus node dysfunction in absence of pacemaker
    boolean
    C0428908 (UMLS CUI [1])
    C0030163 (UMLS CUI [2,1])
    C0332197 (UMLS CUI [2,2])
    Aggrenox | Aspirin | Dipyridamole | Pentoxifylline | Trental | Dipyridamole Oral [Persantine]
    Item
    use of aggrenox (asa/dipyridamole), pentoxifylline (trental) , or oral dipyridamole (persantine)
    boolean
    C0732282 (UMLS CUI [1])
    C0004057 (UMLS CUI [2])
    C0012582 (UMLS CUI [3])
    C0030899 (UMLS CUI [4])
    C0699487 (UMLS CUI [5])
    C1242076 (UMLS CUI [6])
    Atrial Fibrillation
    Item
    atrial fibrillation
    boolean
    C0004238 (UMLS CUI [1])
    Pregnancy | Breast Feeding
    Item
    pregnant/breast feeding
    boolean
    C0032961 (UMLS CUI [1])
    C0006147 (UMLS CUI [2])
    Lacking Able to speak English Language
    Item
    non english speaking patients
    boolean
    C0332268 (UMLS CUI [1,1])
    C0564215 (UMLS CUI [1,2])
    C0376245 (UMLS CUI [1,3])
    Aminophylline allergy | Intolerance to Aminophylline | Hypersensitivity Regadenoson | Intolerance to Regadenoson
    Item
    subject is allergic or intolerant to aminophylline, regadenoson
    boolean
    C0571074 (UMLS CUI [1])
    C1744706 (UMLS CUI [2,1])
    C0002575 (UMLS CUI [2,2])
    C0020517 (UMLS CUI [3,1])
    C1698215 (UMLS CUI [3,2])
    C1744706 (UMLS CUI [4,1])
    C1698215 (UMLS CUI [4,2])
    Lung disease Bronchial Spasm | Bronchial Spasm Suspected | Asthma | Wheezing | Chronic Obstructive Airway Disease
    Item
    subject has a history of known or suspected bronchospastic lung disease [e.g., asthma, wheezing, chronic obstructive pulmonary disease (copd, etc.)]
    boolean
    C0024115 (UMLS CUI [1,1])
    C0006266 (UMLS CUI [1,2])
    C0006266 (UMLS CUI [2,1])
    C0750491 (UMLS CUI [2,2])
    C0004096 (UMLS CUI [3])
    C0043144 (UMLS CUI [4])
    C0024117 (UMLS CUI [5])
    First degree atrioventricular block | Second degree atrioventricular block
    Item
    patients with first degree or second degree av block
    boolean
    C0085614 (UMLS CUI [1])
    C0264906 (UMLS CUI [2])
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