0 Evaluaciones
ID

35098

Descripción

Computed Tomography and Biomarker Analysis in Diagnosing Coronary Artery Disease in Asymptomatic Patients Who Have Undergone Stem Cell Transplant; ODM derived from: https://clinicaltrials.gov/show/NCT02077218

Link

https://clinicaltrials.gov/show/NCT02077218

Palabras clave

Versiones (2)
  1. 2/16/19 2/16/19 -
  2. 2/16/19 2/16/19 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

February 16, 2019

DOI

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Licencia

Creative Commons BY 4.0
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    Eligibility Cancer Survivor NCT02077218

    Inglés

    Eligibility Cancer Survivor NCT02077218

    1 formularios  
    Inclusion Criteria
    Descripción

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    alive and in complete remission at time of enrollment
    Descripción

    Alive | In complete remission

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C2584946
    UMLS CUI [2]
    C0677874
    underwent allogeneic hct after 1995
    Descripción

    Allogeneic Hematopoietic Stem Cell Transplantation

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C1705576
    time between hct and study entry: >= 2 years
    Descripción

    Allogeneic Hematopoietic Stem Cell Transplantation Time Interval Enrollment in clinical trial

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C1705576
    UMLS CUI [1,2]
    C0872291
    UMLS CUI [1,3]
    C4041024
    have at least one cvrf (hypertension, diabetes, dyslipidemia) at the time of eligibility determination
    Descripción

    Cardiovascular risk factors Quantity | Hypertensive disease | Diabetes Mellitus | Dyslipidemia

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0850624
    UMLS CUI [1,2]
    C1265611
    UMLS CUI [2]
    C0020538
    UMLS CUI [3]
    C0011849
    UMLS CUI [4]
    C0242339
    Exclusion Criteria
    Descripción

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    history of ischemic heart disease, stroke, or cardiomyopathy/congestive heart failure
    Descripción

    Myocardial Ischemia | Cerebrovascular accident | Cardiomyopathy | Congestive heart failure

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0151744
    UMLS CUI [2]
    C0038454
    UMLS CUI [3]
    C0878544
    UMLS CUI [4]
    C0018802
    abnormal renal function (glomerular filtration rate [gfr] < 60 ml/min/1.73m2)
    Descripción

    Abnormal renal function | Glomerular Filtration Rate

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0151746
    UMLS CUI [2]
    C0017654
    pregnancy
    Descripción

    Pregnancy

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0032961
    known allergy to intravenous (iv) contrast
    Descripción

    Allergy to intravenous contrast media

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C2242530
    sustained or symptomatic ventricular dysrhythmias uncontrolled with drug therapy or implantable device; significant conduction defects (i.e.: second or third degree atrioventricular block or sick sinus syndrome)
    Descripción

    Ventricular arrhythmia Sustained | Ventricular arrhythmia Symptomatic | Pharmacotherapy Lacking | Implanted device Lacking | Conduction defects | Second degree atrioventricular block | Complete atrioventricular block | Sick Sinus Syndrome

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0085612
    UMLS CUI [1,2]
    C0443318
    UMLS CUI [2,1]
    C0085612
    UMLS CUI [2,2]
    C0231220
    UMLS CUI [3,1]
    C0013216
    UMLS CUI [3,2]
    C0332268
    UMLS CUI [4,1]
    C0021102
    UMLS CUI [4,2]
    C0332268
    UMLS CUI [5]
    C0264886
    UMLS CUI [6]
    C0264906
    UMLS CUI [7]
    C0151517
    UMLS CUI [8]
    C0037052
    current clinical evidence of moderate-to-severe obstructive pulmonary disease or reactive airway diseases (i.e.: asthma) requiring therapy
    Descripción

    Obstructive Lung Disease Moderate | Obstructive Lung Disease Severe | Reactive airway disease Treatment required for | Asthma

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0600260
    UMLS CUI [1,2]
    C0205081
    UMLS CUI [2,1]
    C0600260
    UMLS CUI [2,2]
    C0205082
    UMLS CUI [3,1]
    C3714497
    UMLS CUI [3,2]
    C0332121
    UMLS CUI [4]
    C0004096
    history of drug sensitivity or allergic reaction to beta-blockers
    Descripción

    BETA BLOCKER ALLERGY

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0741466
    currently taking calcium channel blockers such as verapramil and diltiazem
    Descripción

    Calcium Channel Blockers | Verapamil | Diltiazem

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0006684
    UMLS CUI [2]
    C0042523
    UMLS CUI [3]
    C0012373
    history of unrepaired severe aortic stenosis
    Descripción

    Aortic stenosis, severe | Repair Lacking

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C3806272
    UMLS CUI [2,1]
    C4319951
    UMLS CUI [2,2]
    C0332268
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    Similar models

    Eligibility Cancer Survivor NCT02077218

    1 formularios
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    Alias
    Item Group
    C1512693 (UMLS CUI)
    Alive | In complete remission
    Item
    alive and in complete remission at time of enrollment
    boolean
    C2584946 (UMLS CUI [1])
    C0677874 (UMLS CUI [2])
    Allogeneic Hematopoietic Stem Cell Transplantation
    Item
    underwent allogeneic hct after 1995
    boolean
    C1705576 (UMLS CUI [1])
    Allogeneic Hematopoietic Stem Cell Transplantation Time Interval Enrollment in clinical trial
    Item
    time between hct and study entry: >= 2 years
    boolean
    C1705576 (UMLS CUI [1,1])
    C0872291 (UMLS CUI [1,2])
    C4041024 (UMLS CUI [1,3])
    Cardiovascular risk factors Quantity | Hypertensive disease | Diabetes Mellitus | Dyslipidemia
    Item
    have at least one cvrf (hypertension, diabetes, dyslipidemia) at the time of eligibility determination
    boolean
    C0850624 (UMLS CUI [1,1])
    C1265611 (UMLS CUI [1,2])
    C0020538 (UMLS CUI [2])
    C0011849 (UMLS CUI [3])
    C0242339 (UMLS CUI [4])
    Item Group
    C0680251 (UMLS CUI)
    Myocardial Ischemia | Cerebrovascular accident | Cardiomyopathy | Congestive heart failure
    Item
    history of ischemic heart disease, stroke, or cardiomyopathy/congestive heart failure
    boolean
    C0151744 (UMLS CUI [1])
    C0038454 (UMLS CUI [2])
    C0878544 (UMLS CUI [3])
    C0018802 (UMLS CUI [4])
    Abnormal renal function | Glomerular Filtration Rate
    Item
    abnormal renal function (glomerular filtration rate [gfr] < 60 ml/min/1.73m2)
    boolean
    C0151746 (UMLS CUI [1])
    C0017654 (UMLS CUI [2])
    Pregnancy
    Item
    pregnancy
    boolean
    C0032961 (UMLS CUI [1])
    Allergy to intravenous contrast media
    Item
    known allergy to intravenous (iv) contrast
    boolean
    C2242530 (UMLS CUI [1])
    Ventricular arrhythmia Sustained | Ventricular arrhythmia Symptomatic | Pharmacotherapy Lacking | Implanted device Lacking | Conduction defects | Second degree atrioventricular block | Complete atrioventricular block | Sick Sinus Syndrome
    Item
    sustained or symptomatic ventricular dysrhythmias uncontrolled with drug therapy or implantable device; significant conduction defects (i.e.: second or third degree atrioventricular block or sick sinus syndrome)
    boolean
    C0085612 (UMLS CUI [1,1])
    C0443318 (UMLS CUI [1,2])
    C0085612 (UMLS CUI [2,1])
    C0231220 (UMLS CUI [2,2])
    C0013216 (UMLS CUI [3,1])
    C0332268 (UMLS CUI [3,2])
    C0021102 (UMLS CUI [4,1])
    C0332268 (UMLS CUI [4,2])
    C0264886 (UMLS CUI [5])
    C0264906 (UMLS CUI [6])
    C0151517 (UMLS CUI [7])
    C0037052 (UMLS CUI [8])
    Obstructive Lung Disease Moderate | Obstructive Lung Disease Severe | Reactive airway disease Treatment required for | Asthma
    Item
    current clinical evidence of moderate-to-severe obstructive pulmonary disease or reactive airway diseases (i.e.: asthma) requiring therapy
    boolean
    C0600260 (UMLS CUI [1,1])
    C0205081 (UMLS CUI [1,2])
    C0600260 (UMLS CUI [2,1])
    C0205082 (UMLS CUI [2,2])
    C3714497 (UMLS CUI [3,1])
    C0332121 (UMLS CUI [3,2])
    C0004096 (UMLS CUI [4])
    BETA BLOCKER ALLERGY
    Item
    history of drug sensitivity or allergic reaction to beta-blockers
    boolean
    C0741466 (UMLS CUI [1])
    Calcium Channel Blockers | Verapamil | Diltiazem
    Item
    currently taking calcium channel blockers such as verapramil and diltiazem
    boolean
    C0006684 (UMLS CUI [1])
    C0042523 (UMLS CUI [2])
    C0012373 (UMLS CUI [3])
    Aortic stenosis, severe | Repair Lacking
    Item
    history of unrepaired severe aortic stenosis
    boolean
    C3806272 (UMLS CUI [1])
    C4319951 (UMLS CUI [2,1])
    C0332268 (UMLS CUI [2,2])
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