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ID

22462

Beschrijving

Study part: Concomitant Medication.A Phase 2 Multicenter, Double-blind, Placebo-controlled, Study to to Evaluate the Corticosteroid- sparing effects of Mepolizumab in Subjects with Hypereosinophilic Syndromes (HES) and Evaluate Efficacy and Safety of Mepolizumab in Controlling the Clinical Signs and Symptoms of subjects with HES Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Study ID: 100185, Clinical Study ID:MHE100185.

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Versies (1)
  1. 05-06-17 05-06-17 -
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GlaxoSmithKline

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5 juni 2017

DOI

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Creative Commons BY-NC 3.0
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    Concomitant Medication Mepolizumab HES NCT00086658

    Engels

    Concomitant Medication

    1 Formulieren  
    1. StudyEvent: ODM
      1. Concomitant Medication
    CONCOMITANT MEDICATIONS
    Beschrijving

    CONCOMITANT MEDICATIONS

    Alias
    UMLS CUI-1
    C2347852
    Subject ID
    Beschrijving

    Subject ID

    Datatype

    text

    Alias
    UMLS CUI [1]
    C2348585
    Were any concomitant medications taken by the subject during the study?
    Beschrijving

    Concomitant Medication

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C2347852
    Drug Name
    Beschrijving

    Drug Name

    Datatype

    text

    Alias
    UMLS CUI [1]
    C0013227
    Unit Dose
    Beschrijving

    Dose

    Datatype

    float

    Alias
    UMLS CUI [1]
    C2348070
    Units
    Beschrijving

    Unit Total Daily Dose

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C0439148
    UMLS CUI [1,2]
    C2348070
    Frequency
    Beschrijving

    Frequency

    Datatype

    text

    Alias
    UMLS CUI [1]
    C3476109
    Route
    Beschrijving

    Route

    Datatype

    text

    Alias
    UMLS CUI [1]
    C0013153
    Reason for Medication
    Beschrijving

    Reason for Medication

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C0392360
    UMLS CUI [1,2]
    C0013227
    Start Date
    Beschrijving

    Start Date

    Datatype

    date

    Alias
    UMLS CUI [1]
    C0808070
    Stop Date
    Beschrijving

    Stop Date

    Datatype

    date

    Alias
    UMLS CUI [1]
    C0806020
    Ongoing Medication?
    Beschrijving

    Ongoing Medication

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C2826666
    Terug naar het begin van de pagina

    Similar models

    Concomitant Medication

    1 Formulieren
    1. StudyEvent: ODM
      1. Concomitant Medication
    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    CONCOMITANT MEDICATIONS
    C2347852 (UMLS CUI-1)
    Subject ID
    Item
    Subject ID
    text
    C2348585 (UMLS CUI [1])
    Concomitant Medication
    Item
    Were any concomitant medications taken by the subject during the study?
    boolean
    C2347852 (UMLS CUI [1])
    Drug Name
    Item
    Drug Name
    text
    C0013227 (UMLS CUI [1])
    Dose
    Item
    Unit Dose
    float
    C2348070 (UMLS CUI [1])
    Unit Total Daily Dose
    Item
    Units
    text
    C0439148 (UMLS CUI [1,1])
    C2348070 (UMLS CUI [1,2])
    Frequency
    Item
    Frequency
    text
    C3476109 (UMLS CUI [1])
    Route
    Item
    Route
    text
    C0013153 (UMLS CUI [1])
    Reason for Medication
    Item
    Reason for Medication
    text
    C0392360 (UMLS CUI [1,1])
    C0013227 (UMLS CUI [1,2])
    Start Date
    Item
    Start Date
    date
    C0808070 (UMLS CUI [1])
    Stop Date
    Item
    Stop Date
    date
    C0806020 (UMLS CUI [1])
    Ongoing Medication
    Item
    Ongoing Medication?
    boolean
    C2826666 (UMLS CUI [1])
    Terug naar het begin van de pagina 

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