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ID

30893

Descrizione

Study part: Logs and Repeats (Logs/Rpts). A phase 1 single-masked, randomized (with respect to placebo), placebo-controlled, parallel-group, dose-rising study to evaluate the safety, tolerability and pharmacokinetics of repeat oral doses of GW786034 in elderly healthy volunteers. Trade Name: Votrient. Clinical Study ID: MD1103367.

Keywords

  1. 02/07/18 02/07/18 -
Titolare del copyright

GlaxoSmithKline

Caricato su

2 luglio 2018

DOI

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Licenza

Creative Commons BY-NC 3.0

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    Logs and Repeats (Logs/Rpts) Pazopanib Macular Degeneration MD1103367

    Logs and Repeats (Logs/Rpts)

    DATE OF VISIT/ASSESSMENT
    Descrizione

    DATE OF VISIT/ASSESSMENT

    Alias
    UMLS CUI-1
    C1320303
    Date of visit/assessment
    Descrizione

    Date of visit

    Tipo di dati

    date

    Alias
    UMLS CUI [1]
    C1320303
    ADVERSE EVENT/CONCOMITANT MEDICATION/REPEAT ASSESSMENT CHECK QUESTIONS
    Descrizione

    ADVERSE EVENT/CONCOMITANT MEDICATION/REPEAT ASSESSMENT CHECK QUESTIONS

    Alias
    UMLS CUI-1
    C0877248
    UMLS CUI-3
    C2347852
    UMLS CUI-5
    C0681799
    Were any concomitant medications taken by the subject during the study?
    Descrizione

    concomitant medication

    Tipo di dati

    text

    Alias
    UMLS CUI [1]
    C2347852
    Did the subject experience any adverse events during the study?
    Descrizione

    adverse events

    Tipo di dati

    text

    Alias
    UMLS CUI [1]
    C0877248
    Were any repeat haematology or clinical chemistry samples taken?
    Descrizione

    hematology; clinical chemistry

    Tipo di dati

    text

    Alias
    UMLS CUI [1]
    C0474523
    UMLS CUI [2]
    C0008000
    Were any repeat urinalysis sample taken?
    Descrizione

    urinalysis

    Tipo di dati

    text

    Alias
    UMLS CUI [1]
    C0042014
    Were any repeat ECGs performed?
    Descrizione

    ECG

    Tipo di dati

    text

    Alias
    UMLS CUI [1]
    C1623258
    Were any repeat vital signs recorded?
    Descrizione

    vital signs

    Tipo di dati

    text

    Alias
    UMLS CUI [1]
    C0518766

    Similar models

    Logs and Repeats (Logs/Rpts)

    Name
    genere
    Description | Question | Decode (Coded Value)
    Tipo di dati
    Alias
    Item Group
    DATE OF VISIT/ASSESSMENT
    C1320303 (UMLS CUI-1)
    Date of visit
    Item
    Date of visit/assessment
    date
    C1320303 (UMLS CUI [1])
    Item Group
    ADVERSE EVENT/CONCOMITANT MEDICATION/REPEAT ASSESSMENT CHECK QUESTIONS
    C0877248 (UMLS CUI-1)
    C2347852 (UMLS CUI-3)
    C0681799 (UMLS CUI-5)
    Item
    Were any concomitant medications taken by the subject during the study?
    text
    C2347852 (UMLS CUI [1])
    Code List
    Were any concomitant medications taken by the subject during the study?
    CL Item
    Yes (Y)
    CL Item
    No (N)
    Item
    Did the subject experience any adverse events during the study?
    text
    C0877248 (UMLS CUI [1])
    Code List
    Did the subject experience any adverse events during the study?
    CL Item
    Yes (Y)
    CL Item
    No (N)
    Item
    Were any repeat haematology or clinical chemistry samples taken?
    text
    C0474523 (UMLS CUI [1])
    C0008000 (UMLS CUI [2])
    Code List
    Were any repeat haematology or clinical chemistry samples taken?
    CL Item
    Yes (Y)
    CL Item
    No (N)
    Item
    Were any repeat urinalysis sample taken?
    text
    C0042014 (UMLS CUI [1])
    Code List
    Were any repeat urinalysis sample taken?
    CL Item
    Yes (Y)
    CL Item
    No (N)
    Item
    Were any repeat ECGs performed?
    text
    C1623258 (UMLS CUI [1])
    Code List
    Were any repeat ECGs performed?
    CL Item
    Yes (Y)
    CL Item
    No (N)
    Item
    Were any repeat vital signs recorded?
    text
    C0518766 (UMLS CUI [1])
    Code List
    Were any repeat vital signs recorded?
    CL Item
    Yes (Y)
    CL Item
    No (N)

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