0 Evaluaciones
ID

33856

Descripción

Effects of Remote Ischemic Conditioning on Myocardial Perfusion in Humans; ODM derived from: https://clinicaltrials.gov/show/NCT02230098

Link

https://clinicaltrials.gov/show/NCT02230098

Palabras clave

Versiones (1)
  1. 2019-01-04 2019-01-04 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

4 januari 2019

DOI

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Licencia

Creative Commons BY 4.0
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    Eligibility Ischemic Heart Disease NCT02230098

    Inglés

    Eligibility Ischemic Heart Disease NCT02230098

    1 formularios  
    Inclusion Criteria
    Descripción

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693 (Inclusion)
    patients referred for routine myocardial rb82-pet scanning at dept. of nuclear medicine & pet center, aarhus university hospital, skejby, denmark.
    Descripción

    RB-82 PET scan Myocardial

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C1268555 (rubidium chloride Rb-82)
    SNOMED
    129503007
    UMLS CUI [1,2]
    C0032743 (Positron-Emission Tomography)
    SNOMED
    363678002
    LOINC
    LP208893-0
    UMLS CUI [1,3]
    C1522564 (Myocardial)
    able to understand the written patient information and to give informed consent.
    Descripción

    Comprehension Patient Information | Informed Consent

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0162340 (Comprehension)
    SNOMED
    66216009
    UMLS CUI [1,2]
    C1955348 (Patient Information)
    UMLS CUI [2]
    C0021430 (Informed Consent)
    Exclusion Criteria
    Descripción

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251 (Exclusion Criteria)
    patients not undergoing rb82-pet with adenosine stress test.
    Descripción

    RB-82 PET scan Absent | Stress test with adenosine Absent

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C1268555 (rubidium chloride Rb-82)
    SNOMED
    129503007
    UMLS CUI [1,2]
    C0032743 (Positron-Emission Tomography)
    SNOMED
    363678002
    LOINC
    LP208893-0
    UMLS CUI [1,3]
    C0332197 (Absent)
    SNOMED
    2667000
    LOINC
    LA9634-2
    UMLS CUI [2,1]
    C2036185 (pharmacologic stress test with adenosine)
    UMLS CUI [2,2]
    C0332197 (Absent)
    SNOMED
    2667000
    LOINC
    LA9634-2
    strenuous exercise (running, bicycling, fitness), intake of beta-blockers or alcohol intake on the day before and on the day of investigation.
    Descripción

    Strenuous Exercise | Running | Bicycling | Fitness | Adrenergic beta-1 Receptor Antagonists | Alcohol consumption

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C1514989 (Strenuous Exercise)
    UMLS CUI [2]
    C0035953 (Running (physical activity))
    SNOMED
    418060005
    LOINC
    LA11836-6
    UMLS CUI [3]
    C0005377 (Bicycling (recreational activity))
    LOINC
    LA11837-4
    UMLS CUI [4]
    C1456706 (Fitness)
    UMLS CUI [5]
    C0304516 (Adrenergic beta-1 Receptor Antagonists)
    SNOMED
    372661004
    UMLS CUI [6]
    C0001948 (Alcohol consumption)
    SNOMED
    897148007
    LOINC
    MTHU047472
    pregnant/nursing women.
    Descripción

    Pregnancy | Breast Feeding

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0032961 (Pregnancy)
    SNOMED
    289908002
    LOINC
    LP75920-6
    UMLS CUI [2]
    C0006147 (Breast Feeding)
    SNOMED
    169741004
    LOINC
    LP420040-0
    fertile women not using contraceptives.
    Descripción

    Childbearing Potential Contraceptives Absent

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C3831118 (Childbearing Potential)
    UMLS CUI [1,2]
    C0009871 (Contraceptive Agents)
    SNOMED
    108899006
    UMLS CUI [1,3]
    C0332197 (Absent)
    SNOMED
    2667000
    LOINC
    LA9634-2
    patients in dialysis treatment.
    Descripción

    Dialysis

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0011946 (Dialysis procedure)
    SNOMED
    108241001
    other concomitant disease or treatment that according to the investigator's assessment makes the patient unsuitable for study participation.
    Descripción

    Comorbidity Study Subject Participation Status Inappropriate | Therapeutic procedure Study Subject Participation Status Inappropriate

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0009488 (Comorbidity)
    UMLS CUI [1,2]
    C2348568 (Study Subject Participation Status)
    UMLS CUI [1,3]
    C1548788 (Inappropriate)
    UMLS CUI [2,1]
    C0087111 (Therapeutic procedure)
    SNOMED
    277132007
    LOINC
    LP21090-3
    UMLS CUI [2,2]
    C2348568 (Study Subject Participation Status)
    UMLS CUI [2,3]
    C1548788 (Inappropriate)
    known type 2 diabetes
    Descripción

    Diabetes Mellitus, Non-Insulin-Dependent

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0011860 (Diabetes Mellitus, Non-Insulin-Dependent)
    SNOMED
    44054006
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    Similar models

    Eligibility Ischemic Heart Disease NCT02230098

    1 formularios
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    Alias
    Item Group
    C1512693 (UMLS CUI)
    RB-82 PET scan Myocardial
    Item
    patients referred for routine myocardial rb82-pet scanning at dept. of nuclear medicine & pet center, aarhus university hospital, skejby, denmark.
    boolean
    C1268555 (UMLS CUI [1,1])
    C0032743 (UMLS CUI [1,2])
    C1522564 (UMLS CUI [1,3])
    Comprehension Patient Information | Informed Consent
    Item
    able to understand the written patient information and to give informed consent.
    boolean
    C0162340 (UMLS CUI [1,1])
    C1955348 (UMLS CUI [1,2])
    C0021430 (UMLS CUI [2])
    Item Group
    C0680251 (UMLS CUI)
    RB-82 PET scan Absent | Stress test with adenosine Absent
    Item
    patients not undergoing rb82-pet with adenosine stress test.
    boolean
    C1268555 (UMLS CUI [1,1])
    C0032743 (UMLS CUI [1,2])
    C0332197 (UMLS CUI [1,3])
    C2036185 (UMLS CUI [2,1])
    C0332197 (UMLS CUI [2,2])
    Strenuous Exercise | Running | Bicycling | Fitness | Adrenergic beta-1 Receptor Antagonists | Alcohol consumption
    Item
    strenuous exercise (running, bicycling, fitness), intake of beta-blockers or alcohol intake on the day before and on the day of investigation.
    boolean
    C1514989 (UMLS CUI [1])
    C0035953 (UMLS CUI [2])
    C0005377 (UMLS CUI [3])
    C1456706 (UMLS CUI [4])
    C0304516 (UMLS CUI [5])
    C0001948 (UMLS CUI [6])
    Pregnancy | Breast Feeding
    Item
    pregnant/nursing women.
    boolean
    C0032961 (UMLS CUI [1])
    C0006147 (UMLS CUI [2])
    Childbearing Potential Contraceptives Absent
    Item
    fertile women not using contraceptives.
    boolean
    C3831118 (UMLS CUI [1,1])
    C0009871 (UMLS CUI [1,2])
    C0332197 (UMLS CUI [1,3])
    Dialysis
    Item
    patients in dialysis treatment.
    boolean
    C0011946 (UMLS CUI [1])
    Comorbidity Study Subject Participation Status Inappropriate | Therapeutic procedure Study Subject Participation Status Inappropriate
    Item
    other concomitant disease or treatment that according to the investigator's assessment makes the patient unsuitable for study participation.
    boolean
    C0009488 (UMLS CUI [1,1])
    C2348568 (UMLS CUI [1,2])
    C1548788 (UMLS CUI [1,3])
    C0087111 (UMLS CUI [2,1])
    C2348568 (UMLS CUI [2,2])
    C1548788 (UMLS CUI [2,3])
    Diabetes Mellitus, Non-Insulin-Dependent
    Item
    known type 2 diabetes
    boolean
    C0011860 (UMLS CUI [1])
    Volver a la parte superior de la página 

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