0 Beoordelingen
ID

33856

Beschrijving

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

Link

https://clinicaltrials.gov/show/NCT02230098

Trefwoorden

Versies (1)
  1. 04-01-19 04-01-19 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

4 januari 2019

DOI

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Licentie

Creative Commons BY 4.0
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    Eligibility Ischemic Heart Disease NCT02230098

    Engels

    Eligibility Ischemic Heart Disease NCT02230098

    1 Formulieren  
    Inclusion Criteria
    Beschrijving

    Inclusion Criteria

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

    RB-82 PET scan Myocardial

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C1268555
    UMLS CUI [1,2]
    C0032743
    UMLS CUI [1,3]
    C1522564
    able to understand the written patient information and to give informed consent.
    Beschrijving

    Comprehension Patient Information | Informed Consent

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0162340
    UMLS CUI [1,2]
    C1955348
    UMLS CUI [2]
    C0021430
    Exclusion Criteria
    Beschrijving

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    patients not undergoing rb82-pet with adenosine stress test.
    Beschrijving

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

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C1268555
    UMLS CUI [1,2]
    C0032743
    UMLS CUI [1,3]
    C0332197
    UMLS CUI [2,1]
    C2036185
    UMLS CUI [2,2]
    C0332197
    strenuous exercise (running, bicycling, fitness), intake of beta-blockers or alcohol intake on the day before and on the day of investigation.
    Beschrijving

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

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C1514989
    UMLS CUI [2]
    C0035953
    UMLS CUI [3]
    C0005377
    UMLS CUI [4]
    C1456706
    UMLS CUI [5]
    C0304516
    UMLS CUI [6]
    C0001948
    pregnant/nursing women.
    Beschrijving

    Pregnancy | Breast Feeding

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0032961
    UMLS CUI [2]
    C0006147
    fertile women not using contraceptives.
    Beschrijving

    Childbearing Potential Contraceptives Absent

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C3831118
    UMLS CUI [1,2]
    C0009871
    UMLS CUI [1,3]
    C0332197
    patients in dialysis treatment.
    Beschrijving

    Dialysis

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0011946
    other concomitant disease or treatment that according to the investigator's assessment makes the patient unsuitable for study participation.
    Beschrijving

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

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0009488
    UMLS CUI [1,2]
    C2348568
    UMLS CUI [1,3]
    C1548788
    UMLS CUI [2,1]
    C0087111
    UMLS CUI [2,2]
    C2348568
    UMLS CUI [2,3]
    C1548788
    known type 2 diabetes
    Beschrijving

    Diabetes Mellitus, Non-Insulin-Dependent

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0011860
    Terug naar het begin van de pagina

    Similar models

    Eligibility Ischemic Heart Disease NCT02230098

    1 Formulieren
    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    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])
    Terug naar het begin van de pagina 

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