ID

16595

Descripción

MIPSO Comparative study of bacterial microbiota in the skin and intestines of psoriasis patients before and after systemic treatment with adalimumab or ustekinumab or ciclosporin (EudraCT 2014-003022-40) Principal Investigator: Prof. Dr. Dr. H. C. Thomas A. Luger

Palabras clave

  1. 08/12/2015 08/12/2015 -
  2. 25/07/2016 25/07/2016 -
Subido en

25 juillet 2016

DOI

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Licencia

Creative Commons BY-NC 3.0

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    End of Study Psoriasis MIPSO EudraCT 2014-003022-40 DRKS00007147

    End of Study Psoriasis MIPSO EudraCT 2014-003022-40

    End of Study
    Descripción

    End of Study

    Alias
    UMLS CUI-1
    C0444496
    Patient number
    Descripción

    Patient number

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C1830427
    Date end of study
    Descripción

    Date end of study

    Tipo de datos

    date

    Alias
    UMLS CUI [1]
    C2983670
    End of Study
    Descripción

    End of Study

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C0444496
    Early Study termination
    Descripción

    Early Study termination (if more than one, specify below)

    Tipo de datos

    integer

    Alias
    UMLS CUI [1]
    C2718058
    End of Study Reason
    Descripción

    End of Study Reason

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C0444496
    UMLS CUI [1,2]
    C0392360

    Similar models

    End of Study Psoriasis MIPSO EudraCT 2014-003022-40

    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    Alias
    Item Group
    End of Study
    C0444496 (UMLS CUI-1)
    Patient number
    Item
    text
    C1830427 (UMLS CUI [1])
    Date end of study
    Item
    date
    C2983670 (UMLS CUI [1])
    Item
    text
    C0444496 (UMLS CUI [1])
    Code List
    End of Study
    CL Item
    regular end of study (1)
    CL Item
    early study termination (2)
    Item
    Early Study termination
    integer
    C2718058 (UMLS CUI [1])
    Code List
    Early Study termination
    CL Item
    Change of treatment required (1)
    CL Item
    Patient's request (2)
    CL Item
    Inclusion/exclusion criteria were injured, before initializing therapy (3)
    CL Item
    Inclusion/exclusion criteria were injured, after initializing therapy (4)
    CL Item
    Entering pregnancy (5)
    CL Item
    Disallowed concomitant medication required (6)
    CL Item
    The continued participation in the clinical trial is medically no longer justifiable (7)
    CL Item
    Time windows for visits could not be complied with (8)
    CL Item
    Lack of patient compliance (9)
    CL Item
    Cancelation of the entire study (10)
    CL Item
    other reason (11)
    End of Study Reason
    Item
    text
    C0444496 (UMLS CUI [1,1])
    C0392360 (UMLS CUI [1,2])

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