0 Ratings
ID

38643

Description

Study ID: 109035 Clinical Study ID: 109035 Study Title: A Randomised, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy and Safety of GSK163090 in Subjects With Major Depressive Disorder Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00896363 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: GSK163090 1 mg, GSK163090 Placebo, GSK163090 3 mg Trade Name: Study Indication: Depressive Disorder

Keywords

Versions (1)
  1. 10/29/19 10/29/19 -
Copyright Holder

GlaxoSmithKline

Uploaded on

October 29, 2019

DOI

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License

Creative Commons BY-NC 3.0
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    Efficacy and Safety of GSK163090 in Subjects with Major Depressive Disorder; NCT00896363

    English

    Investigational Product

    1 forms  
    AM Dose
    Description

    AM Dose

    Alias
    UMLS CUI-1
    C0304229
    UMLS CUI-2
    C0178602
    UMLS CUI-3
    C0332170
    Date/time of dose
    Description

    Experimental drug, Dosage, Morning, Date in time, Time

    Data type

    datetime

    Alias
    UMLS CUI [1,1]
    C0304229
    UMLS CUI [1,2]
    C0178602
    UMLS CUI [1,3]
    C0332170
    UMLS CUI [1,4]
    C0011008
    UMLS CUI [1,5]
    C0040223
    PM Dose
    Description

    PM Dose

    Alias
    UMLS CUI-1
    C0304229
    UMLS CUI-2
    C0178602
    UMLS CUI-3
    C0587117
    Date/time of dose
    Description

    Experimental drug, Dosage, Evening, Date in time, Time

    Data type

    datetime

    Alias
    UMLS CUI [1,1]
    C0304229
    UMLS CUI [1,2]
    C0178602
    UMLS CUI [1,3]
    C0587117
    UMLS CUI [1,4]
    C0011008
    UMLS CUI [1,5]
    C0040223
    Treatment Confirmation
    Description

    Treatment Confirmation

    Alias
    UMLS CUI-1
    C0087111
    UMLS CUI-2
    C0750484
    Did the subject receive the correct treatment (e.g., treatment which the subject was assigned to) during this dosing interval?
    Description

    Therapeutic procedure, Correct

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0087111
    UMLS CUI [1,2]
    C2349182
    No, record reason(s)
    Description

    Therapeutic procedure, Wrong, Reason and justification

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0087111
    UMLS CUI [1,2]
    C3827420
    UMLS CUI [1,3]
    C0566251
    Back to the top of the page

    Similar models

    Investigational Product

    1 forms
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    AM Dose
    C0304229 (UMLS CUI-1)
    C0178602 (UMLS CUI-2)
    C0332170 (UMLS CUI-3)
    Experimental drug, Dosage, Morning, Date in time, Time
    Item
    Date/time of dose
    datetime
    C0304229 (UMLS CUI [1,1])
    C0178602 (UMLS CUI [1,2])
    C0332170 (UMLS CUI [1,3])
    C0011008 (UMLS CUI [1,4])
    C0040223 (UMLS CUI [1,5])
    Item Group
    PM Dose
    C0304229 (UMLS CUI-1)
    C0178602 (UMLS CUI-2)
    C0587117 (UMLS CUI-3)
    Experimental drug, Dosage, Evening, Date in time, Time
    Item
    Date/time of dose
    datetime
    C0304229 (UMLS CUI [1,1])
    C0178602 (UMLS CUI [1,2])
    C0587117 (UMLS CUI [1,3])
    C0011008 (UMLS CUI [1,4])
    C0040223 (UMLS CUI [1,5])
    Item Group
    Treatment Confirmation
    C0087111 (UMLS CUI-1)
    C0750484 (UMLS CUI-2)
    Therapeutic procedure, Correct
    Item
    Did the subject receive the correct treatment (e.g., treatment which the subject was assigned to) during this dosing interval?
    boolean
    C0087111 (UMLS CUI [1,1])
    C2349182 (UMLS CUI [1,2])
    Therapeutic procedure, Wrong, Reason and justification
    Item
    No, record reason(s)
    text
    C0087111 (UMLS CUI [1,1])
    C3827420 (UMLS CUI [1,2])
    C0566251 (UMLS CUI [1,3])
    Back to the top of the page 

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