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ID

22498

Description

Study part: Rotterdem Symptom Checklist (RSCL) Week 38.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.

Keywords

  1. 6/5/17 6/5/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

June 5, 2017

DOI

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License

Creative Commons BY-NC 3.0

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    Rotterdem Symptom Checklist (RSCL) Week 38 Mepolizumab HES NCT00086658

    Rotterdem Symptom Checklist (RSCL) Week 38

    Rotterdem Symptom Checklist (RSCL)
    Description

    Rotterdem Symptom Checklist (RSCL)

    Alias
    UMLS CUI-1
    C0451524 (Symptom checklist)
    SNOMED
    273859002
    Subject ID
    Description

    Subject ID

    Data type

    text

    Alias
    UMLS CUI [1]
    C2348585 (Clinical Trial Subject Unique Identifier)
    Rotterdem Symptom Checklist (RSCL) score
    Description

    Symptom checklist Score

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0451524 (Symptom checklist)
    SNOMED
    273859002
    UMLS CUI [1,2]
    C0449820 (Score)
    SNOMED
    246262008
    LOINC
    MTHU024701

    Similar models

    Rotterdem Symptom Checklist (RSCL) Week 38

    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    Rotterdem Symptom Checklist (RSCL)
    C0451524 (UMLS CUI-1)
    Subject ID
    Item
    Subject ID
    text
    C2348585 (UMLS CUI [1])
    Symptom checklist Score
    Item
    Rotterdem Symptom Checklist (RSCL) score
    text
    C0451524 (UMLS CUI [1,1])
    C0449820 (UMLS CUI [1,2])

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