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ID

22452

Beschrijving

Study part: Central Laboratory Screening Visit.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. 04/06/2017 04/06/2017 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

4 juin 2017

DOI

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Licentie

Creative Commons BY-NC 3.0

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    Central Laboratory Screening Visit Mepolizumab HES NCT00086658

    Central Laboratory Screening Visit

    CENTRAL LABORATORY - BLOOD
    Beschrijving

    CENTRAL LABORATORY - BLOOD

    Alias
    UMLS CUI-1
    C0022877 (Laboratory)
    SNOMED
    261904005
    LOINC
    MTHU029808
    Subject ID
    Beschrijving

    Subject ID

    Datatype

    text

    Alias
    UMLS CUI [1]
    C2348585 (Clinical Trial Subject Unique Identifier)
    Date sample taken
    Beschrijving

    Date sample taken

    Datatype

    date

    Alias
    UMLS CUI [1]
    C1302413 (Specimen collection date)
    SNOMED
    399445004
    SERUM PREGNANCY TEST PROMPT
    Beschrijving

    SERUM PREGNANCY TEST PROMPT

    Alias
    UMLS CUI-1
    C0430060 (Serum pregnancy test (B-HCG))
    SNOMED
    166434005
    SERUM PREGNANCY TEST
    Beschrijving

    If subject is female and of childbearing potential a serum pregnancy test must be performed.

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0430060 (Serum pregnancy test (B-HCG))
    SNOMED
    166434005
    SUBJECT REGISTRATION
    Beschrijving

    SUBJECT REGISTRATION

    Alias
    UMLS CUI-1
    C1514821 (Registration)
    SUBJECT REGISTRATION
    Beschrijving

    Ensure that subject is registered in Covance IVRS.

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C1514821 (Registration)

    Similar models

    Central Laboratory Screening Visit

    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    CENTRAL LABORATORY - BLOOD
    C0022877 (UMLS CUI-1)
    Subject ID
    Item
    Subject ID
    text
    C2348585 (UMLS CUI [1])
    Date sample taken
    Item
    Date sample taken
    date
    C1302413 (UMLS CUI [1])
    Item Group
    SERUM PREGNANCY TEST PROMPT
    C0430060 (UMLS CUI-1)
    SERUM PREGNANCY TEST
    Item
    SERUM PREGNANCY TEST
    boolean
    C0430060 (UMLS CUI [1])
    Item Group
    SUBJECT REGISTRATION
    C1514821 (UMLS CUI-1)
    REGISTRATION
    Item
    SUBJECT REGISTRATION
    boolean
    C1514821 (UMLS CUI [1])

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