0 Évaluations

ID

5081

Description

ODM derived from http://clinicaltrials.gov/show/NCT01094678

Lien

http://clinicaltrials.gov/show/NCT01094678

Mots-clés

  1. 06/12/2013 06/12/2013 - Martin Dugas
  2. 17/04/2014 17/04/2014 - Julian Varghese
Téléchargé le

17 avril 2014

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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    Eligibility NCT01094678 Peripheral Arterial Disease

    Eligibility

    1. StudyEvent: Eligibility
      1. Eligibility
    Einschlusskriterien
    Description

    Einschlusskriterien

    Alias
    UMLS CUI 2011AA
    CL425202
    Alter mindestens 18 Jahre
    Description

    age at least 18 Years

    Type de données

    boolean

    Alias
    UMLS CUI 2011AA
    C0001779
    SNOMED CT 2011_0131
    397669002
    stenosis of the above-the-knee femoropopliteal artery
    Description

    stenosis of the above-the-knee femoropopliteal artery

    Type de données

    boolean

    Alias
    UMLS CUI 2011AA
    C2721556
    MedDRA 14.1
    10069344
    UMLS CUI 2011AA
    C0011900
    SNOMED CT 2011_0131
    439401001
    LOINC Version 232
    MTHU008876
    UMLS CUI 2011AA
    CL384738
    UMLS CUI 2011AA
    C0022742
    SNOMED CT 2011_0131
    304679005
    LOINC Version 232
    MTHU002687
    appropriate size and location of the lesion
    Description

    appropriate size and location of the lesion

    Type de données

    boolean

    Alias
    UMLS CUI 2011AA
    C0814634
    UMLS CUI 2011AA
    C0449453
    SNOMED CT 2011_0131
    246116008
    UMLS CUI 2011AA
    C0450429
    SNOMED CT 2011_0131
    246267002
    UMLS CUI 2011AA
    C0221198
    SNOMED CT 2011_0131
    49755003
    Ausschlusskriterien
    Description

    Ausschlusskriterien

    Alias
    UMLS CUI 2011AA
    CL425201
    pregnant or breast feeding
    Description

    pregnant or breast feeding

    Type de données

    boolean

    Alias
    UMLS CUI 2011AA
    C0549206
    MedDRA 14.1
    10036586
    UMLS CUI 2011AA
    C0006147
    MedDRA 14.1
    10006247
    failure or inability to give informed consent
    Description

    failure or inability to give informed consent

    Type de données

    boolean

    Alias
    UMLS CUI 2011AA
    C0021430
    simultaneously participating in another drug or device study
    Description

    simultaneously participating in another drug or device study

    Type de données

    boolean

    Alias
    UMLS CUI 2011AA
    C0521115
    SNOMED CT 2011_0131
    79970003
    UMLS CUI 2011AA
    C0679823
    HL7 V3 2006_05
    PART
    UMLS CUI 2011AA
    C0205394
    SNOMED CT 2011_0131
    74964007
    UMLS CUI 2011AA
    C0013175
    SNOMED CT 2011_0131
    185922005
    UMLS CUI 2011AA
    C2346570
    UMLS CUI 2011AA
    C0008976
    SNOMED CT 2011_0131
    110465008

    Similar models

    Eligibility

    1. StudyEvent: Eligibility
      1. Eligibility
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    Einschlusskriterien
    CL425202 (UMLS CUI 2011AA)
    age at least 18 Years
    Item
    Alter mindestens 18 Jahre
    boolean
    C0001779 (UMLS CUI 2011AA)
    397669002 (SNOMED CT 2011_0131)
    stenosis of the above-the-knee femoropopliteal artery
    Item
    stenosis of the above-the-knee femoropopliteal artery
    boolean
    C2721556 (UMLS CUI 2011AA)
    10069344 (MedDRA 14.1)
    C0011900 (UMLS CUI 2011AA)
    439401001 (SNOMED CT 2011_0131)
    MTHU008876 (LOINC Version 232)
    CL384738 (UMLS CUI 2011AA)
    C0022742 (UMLS CUI 2011AA)
    304679005 (SNOMED CT 2011_0131)
    MTHU002687 (LOINC Version 232)
    appropriate size and location of the lesion
    Item
    appropriate size and location of the lesion
    boolean
    C0814634 (UMLS CUI 2011AA)
    C0449453 (UMLS CUI 2011AA)
    246116008 (SNOMED CT 2011_0131)
    C0450429 (UMLS CUI 2011AA)
    246267002 (SNOMED CT 2011_0131)
    C0221198 (UMLS CUI 2011AA)
    49755003 (SNOMED CT 2011_0131)
    Item Group
    Ausschlusskriterien
    CL425201 (UMLS CUI 2011AA)
    pregnant or breast feeding
    Item
    pregnant or breast feeding
    boolean
    C0549206 (UMLS CUI 2011AA)
    10036586 (MedDRA 14.1)
    C0006147 (UMLS CUI 2011AA)
    10006247 (MedDRA 14.1)
    failure or inability to give informed consent
    Item
    failure or inability to give informed consent
    boolean
    C0021430 (UMLS CUI 2011AA)
    simultaneously participating in another drug or device study
    Item
    simultaneously participating in another drug or device study
    boolean
    C0521115 (UMLS CUI 2011AA)
    79970003 (SNOMED CT 2011_0131)
    C0679823 (UMLS CUI 2011AA)
    PART (HL7 V3 2006_05)
    C0205394 (UMLS CUI 2011AA)
    74964007 (SNOMED CT 2011_0131)
    C0013175 (UMLS CUI 2011AA)
    185922005 (SNOMED CT 2011_0131)
    C2346570 (UMLS CUI 2011AA)
    C0008976 (UMLS CUI 2011AA)
    110465008 (SNOMED CT 2011_0131)

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