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ID

22456

Description

Study part: Pregnancy Information Study Conclusion.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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Versions (1)
  1. 6/5/17 6/5/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

June 5, 2017

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Creative Commons BY-NC 3.0
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    Pregnancy Information Study Conclusion Mepolizumab HES NCT00086658

    English

    Pregnancy Information Study Conclusion

    1 forms  
    PREGNANCY INFORMATION
    Description

    PREGNANCY INFORMATION

    Alias
    UMLS CUI-1
    C0032961 (Pregnancy)
    SNOMED
    289908002
    LOINC
    LP75920-6
    Did the subject become pregnant during the study?
    Description

    pregnancy

    Data type

    text

    Alias
    UMLS CUI [1]
    C0032961 (Pregnancy)
    SNOMED
    289908002
    LOINC
    LP75920-6
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    Similar models

    Pregnancy Information Study Conclusion

    1 forms
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    PREGNANCY INFORMATION
    C0032961 (UMLS CUI-1)
    Item
    Did the subject become pregnant during the study?
    text
    C0032961 (UMLS CUI [1])
    pregnancy
    Code List
    Did the subject become pregnant during the study?
    CL Item
    Yes (If Yes, complete Pregnancy Notification form.) (Yes (If Yes, complete Pregnancy Notification form.))
    CL Item
    No (No)
    CL Item
    Not Applicable (not of childbearing potential or male) (Not Applicable (not of childbearing potential or male))
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