0 Ratings

ID

23833

Description

Study part: 12-Lead ECG Week 38/ Early Withdrawal 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.

Keywords

  1. 7/15/17 7/15/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

July 15, 2017

DOI

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License

Creative Commons BY-NC 3.0

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    12-Lead ECG Week 38 Mepolizumab HES NCT00086658

    12-Lead ECG Week 38

    1. StudyEvent: ODM
      1. 12-Lead ECG Week 38
    12-Lead ECG
    Description

    12-Lead ECG

    Alias
    UMLS CUI-1
    C0430456
    Subject ID
    Description

    Subject ID

    Data type

    text

    Alias
    UMLS CUI [1]
    C2348585
    Visit Date
    Description

    Visit Date

    Data type

    date

    Alias
    UMLS CUI [1]
    C1320303
    Date of ECG
    Description

    Date of ECG

    Data type

    date

    Alias
    UMLS CUI [1]
    C2826640
    Result of the ECG
    Description

    Result of the ECG

    Data type

    text

    Alias
    UMLS CUI [1]
    C0438154

    Similar models

    12-Lead ECG Week 38

    1. StudyEvent: ODM
      1. 12-Lead ECG Week 38
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    12-Lead ECG
    C0430456 (UMLS CUI-1)
    Subject ID
    Item
    Subject ID
    text
    C2348585 (UMLS CUI [1])
    Visit Date
    Item
    Visit Date
    date
    C1320303 (UMLS CUI [1])
    Date of ECG
    Item
    Date of ECG
    date
    C2826640 (UMLS CUI [1])
    Item
    Result of the ECG
    text
    C0438154 (UMLS CUI [1])
    Code List
    Result of the ECG
    CL Item
    Clinically significant change from Baseline favourable (Clinically significant change from Baseline favourable)
    CL Item
    Clinically significant change from Baseline unfavourable (Clinically significant change from Baseline unfavourable)
    CL Item
    No change or insignificant change from Baseline (No change or insignificant change from Baseline)
    CL Item
    No result (not available (No result (not available)

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