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ID

30917

Description

Study part: Study End Day 28. (1,3)-β-D-glucan-based diagnosis of invasive Candida infection versus culture-based diagnosis in patients with severe sepsis or septic shock and at high risk of invasive Candida infection (CandiSep). Provided by PD Dr. med. Frank Bloos, Ph.D. Clinic for Anesthesiology and Intensive care, University Clinic Jena.

Keywords

  1. 5/27/18 5/27/18 -
  2. 7/3/18 7/3/18 -
Copyright Holder

Clinic for Anesthesiology and Intensive care, University Clinic Jena

Uploaded on

July 3, 2018

DOI

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License

Creative Commons BY-NC 3.0

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    Study End Day 28 CandiSep Anesthesiology and Intensive Care NCT02734550

    Study End Day 28

    1. StudyEvent: ODM
      1. Study End Day 28
    Studienende
    Description

    Studienende

    Alias
    UMLS CUI-1
    C0008972
    UMLS CUI-2
    C0444930
    Patienten-ID:
    Description

    Patient ID

    Data type

    text

    Alias
    UMLS CUI [1]
    C2348585
    Datum
    Description

    Date

    Data type

    date

    Alias
    UMLS CUI [1]
    C0011008
    Hat der Patient die Studie vorzeitig beendet?
    Description

    (vor Ablauf von Tag 28 nach Randomisierung)

    Data type

    integer

    Alias
    UMLS CUI [1]
    C2718058
    Vorzeitiges Studienende Datum
    Description

    Date early termination of clinical trial

    Data type

    date

    Alias
    UMLS CUI [1,1]
    C2983670
    UMLS CUI [1,2]
    C2718058
    Grund
    Description

    Study end reason

    Data type

    integer

    Alias
    UMLS CUI [1,1]
    C0444496
    UMLS CUI [1,2]
    C0392360
    Andere Grund
    Description

    Other indication

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0205394
    UMLS CUI [1,2]
    C3146298
    Hat der Patient die Einwilligung zur Probenentnahme für die Biomaterialbank zurückgezogen?
    Description

    consent withdrawn for Specimen Collection

    Data type

    integer

    Alias
    UMLS CUI [1,1]
    C1707492
    UMLS CUI [1,2]
    C0200345
    Falls ja,
    Description

    Specimen collection usage

    Data type

    integer

    Alias
    UMLS CUI [1,1]
    C0200345
    UMLS CUI [1,2]
    C0457083
    Datum Rücknahme
    Description

    date consent withdrawn

    Data type

    date

    Alias
    UMLS CUI [1,1]
    C0011008
    UMLS CUI [1,2]
    C1707492

    Similar models

    Study End Day 28

    1. StudyEvent: ODM
      1. Study End Day 28
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    Studienende
    C0008972 (UMLS CUI-1)
    C0444930 (UMLS CUI-2)
    Patient ID
    Item
    Patienten-ID:
    text
    C2348585 (UMLS CUI [1])
    Date
    Item
    Datum
    date
    C0011008 (UMLS CUI [1])
    Item
    Hat der Patient die Studie vorzeitig beendet?
    integer
    C2718058 (UMLS CUI [1])
    Code List
    Hat der Patient die Studie vorzeitig beendet?
    CL Item
    nein (0)
    CL Item
    ja (1)
    Date early termination of clinical trial
    Item
    Vorzeitiges Studienende Datum
    date
    C2983670 (UMLS CUI [1,1])
    C2718058 (UMLS CUI [1,2])
    Item
    Grund
    integer
    C0444496 (UMLS CUI [1,1])
    C0392360 (UMLS CUI [1,2])
    Code List
    Grund
    CL Item
    Zurückziehen der Einwilligungserklärung durch den Patienten bzw. durch den Betreuer/Bevollmächtigten  (1)
    C4330933 (UMLS CUI-1)
    (Comment:de)
    CL Item
    nach Entscheidung des (Haupt-)Prüfers, wenn die Sicherheit des Patienten nicht mehr gewährleistet ist  (2)
    C0008972 (UMLS CUI-1)
    C0444930 (UMLS CUI-2)
    C0008961 (UMLS CUI-3)
    (Comment:de)
    CL Item
    nach Entscheidung des Sponsorbevollmächtigten  (3)
    C1710224 (UMLS CUI-1)
    (Comment:de)
    CL Item
    Tod  (4)
    C0011065 (UMLS CUI-1)
    (Comment:de)
    CL Item
    Lost to Follow-Up  (5)
    C1302313 (UMLS CUI-1)
    (Comment:de)
    CL Item
    Anderer (6)
    C0205394 (UMLS CUI-1)
    (Comment:de)
    Other indication
    Item
    Andere Grund
    text
    C0205394 (UMLS CUI [1,1])
    C3146298 (UMLS CUI [1,2])
    Item
    Hat der Patient die Einwilligung zur Probenentnahme für die Biomaterialbank zurückgezogen?
    integer
    C1707492 (UMLS CUI [1,1])
    C0200345 (UMLS CUI [1,2])
    Code List
    Hat der Patient die Einwilligung zur Probenentnahme für die Biomaterialbank zurückgezogen?
    CL Item
    nein (0)
    CL Item
    ja (1)
    Item
    Falls ja,
    integer
    C0200345 (UMLS CUI [1,1])
    C0457083 (UMLS CUI [1,2])
    Code List
    Falls ja,
    CL Item
    bisher abgenommene Proben dürfen nicht verwendet werden  (1)
    CL Item
    bisher abgenommene Proben dürfen verwendet werden (2)
    date consent withdrawn
    Item
    Datum Rücknahme
    date
    C0011008 (UMLS CUI [1,1])
    C1707492 (UMLS CUI [1,2])

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