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ID

22461

Beschrijving

Study part: Corticosteroid 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.

Trefwoorden

  1. 05-06-17 05-06-17 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

5 juni 2017

DOI

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Licentie

Creative Commons BY-NC 3.0

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    Corticosteroid Medication Mepolizumab HES NCT00086658

    Corticosteroid Medication

    CORTICOSTEROID MEDICATION
    Beschrijving

    CORTICOSTEROID MEDICATION

    Alias
    UMLS CUI-1
    C0013227 (Pharmaceutical Preparations)
    SNOMED
    763158003
    LOINC
    LP100609-9
    UMLS CUI-2
    C0001617 (Adrenal Cortex Hormones)
    SNOMED
    21568003
    LOINC
    LP20687-7
    Subject ID
    Beschrijving

    Subject ID

    Datatype

    text

    Alias
    UMLS CUI [1]
    C2348585 (Clinical Trial Subject Unique Identifier)
    Was any Corticosteroid medication taken by the subject after the first dose of study medication?
    Beschrijving

    Medication Corticosteroid

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0013227 (Pharmaceutical Preparations)
    SNOMED
    763158003
    LOINC
    LP100609-9
    UMLS CUI [1,2]
    C0001617 (Adrenal Cortex Hormones)
    SNOMED
    21568003
    LOINC
    LP20687-7
    Drug Name
    Beschrijving

    Drug Name

    Datatype

    text

    Alias
    UMLS CUI [1]
    C0013227 (Pharmaceutical Preparations)
    SNOMED
    763158003
    LOINC
    LP100609-9
    Total Daily Dose
    Beschrijving

    Total Daily Dose

    Datatype

    float

    Alias
    UMLS CUI [1]
    C2348070 (Daily Dose)
    Units
    Beschrijving

    Unit Total Daily Dose

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C0439148 (Unit)
    SNOMED
    767525000
    UMLS CUI [1,2]
    C2348070 (Daily Dose)
    Start Date
    Beschrijving

    Start Date

    Datatype

    date

    Alias
    UMLS CUI [1]
    C0808070 (Start Date)
    Stop Date
    Beschrijving

    Stop Date

    Datatype

    date

    Alias
    UMLS CUI [1]
    C0806020 (End date)
    SNOMED
    454551000124105
    LOINC
    MTHU008302
    Ongoing Medication?
    Beschrijving

    Ongoing Medication

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C2826666 (Concomitant Medication Ongoing)

    Similar models

    Corticosteroid Medication

    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    CORTICOSTEROID MEDICATION
    C0013227 (UMLS CUI-1)
    C0001617 (UMLS CUI-2)
    Subject ID
    Item
    Subject ID
    text
    C2348585 (UMLS CUI [1])
    Medication Corticosteroid
    Item
    Was any Corticosteroid medication taken by the subject after the first dose of study medication?
    boolean
    C0013227 (UMLS CUI [1,1])
    C0001617 (UMLS CUI [1,2])
    Drug Name
    Item
    Drug Name
    text
    C0013227 (UMLS CUI [1])
    Total Daily Dose
    Item
    Total Daily Dose
    float
    C2348070 (UMLS CUI [1])
    Unit Total Daily Dose
    Item
    Units
    text
    C0439148 (UMLS CUI [1,1])
    C2348070 (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])

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