0 Ratings
ID

38743

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. 10/31/19 10/31/19 -
Copyright Holder

GlaxoSmithKline

Uploaded on

October 31, 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

    Concomitant Medications

    1 forms  
    Concomitant Medications
    Description

    Concomitant Medications

    Alias
    UMLS CUI-1
    C2347852
    Sequence Number
    Description

    Concomitant Agent, Sequence Number

    Data type

    integer

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C2348184
    Drug name
    Description

    Concomitant Agent, Medication name

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C2360065
    Modified reported term
    Description

    Concomitant Medication Modified Reported Term

    Data type

    text

    Alias
    UMLS CUI [1]
    C2826819
    GSK Drug synonym
    Description

    Concomitant Agent, Pharmaceutical Preparations, Synonym

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0013227
    UMLS CUI [1,3]
    C0871468
    GSK Drug Collection code
    Description

    Concomitant Agent, Pharmaceutical Preparations, Code

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0013227
    UMLS CUI [1,3]
    C0805701
    Failed coding
    Description

    Concomitant Agent, Code, Failed

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0805701
    UMLS CUI [1,3]
    C0231175
    Unit Dose
    Description

    Concomitant Agent, Unit of Measure, Dosage

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C1519795
    UMLS CUI [1,3]
    C0178602
    Units
    Description

    Concomitant Agent, Unit of Measure

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C1519795
    UMLS CUI [1,3]
    C0178602
    Frequency
    Description

    Concomitant Agent, Frequencies

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0439603
    Route
    Description

    Concomitant Agent, Drug Administration Routes

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0013153
    Reason for Medication
    Description

    Concomitant Agent, Reason and justification

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0566251
    Start Date and Time
    Description

    Concomitant Agent, Start Date, Start time

    Data type

    datetime

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0808070
    UMLS CUI [1,3]
    C1301880
    Taken Prior to Study?
    Description

    Concomitant Medication Previous Occurrence

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C2826667
    Ongoing?
    Description

    Concomitant Medication Ongoing

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C2826666
    No, specify End Date and Time
    Description

    Concomitant Agent, End Date, End time

    Data type

    datetime

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0806020
    UMLS CUI [1,3]
    C1522314
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    Similar models

    Concomitant Medications

    1 forms
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    Concomitant Medications
    C2347852 (UMLS CUI-1)
    Concomitant Agent, Sequence Number
    Item
    Sequence Number
    integer
    C2347852 (UMLS CUI [1,1])
    C2348184 (UMLS CUI [1,2])
    Concomitant Agent, Medication name
    Item
    Drug name
    text
    C2347852 (UMLS CUI [1,1])
    C2360065 (UMLS CUI [1,2])
    Concomitant Medication Modified Reported Term
    Item
    Modified reported term
    text
    C2826819 (UMLS CUI [1])
    Concomitant Agent, Pharmaceutical Preparations, Synonym
    Item
    GSK Drug synonym
    text
    C2347852 (UMLS CUI [1,1])
    C0013227 (UMLS CUI [1,2])
    C0871468 (UMLS CUI [1,3])
    Concomitant Agent, Pharmaceutical Preparations, Code
    Item
    GSK Drug Collection code
    text
    C2347852 (UMLS CUI [1,1])
    C0013227 (UMLS CUI [1,2])
    C0805701 (UMLS CUI [1,3])
    Concomitant Agent, Code, Failed
    Item
    Failed coding
    text
    C2347852 (UMLS CUI [1,1])
    C0805701 (UMLS CUI [1,2])
    C0231175 (UMLS CUI [1,3])
    Concomitant Agent, Unit of Measure, Dosage
    Item
    Unit Dose
    text
    C2347852 (UMLS CUI [1,1])
    C1519795 (UMLS CUI [1,2])
    C0178602 (UMLS CUI [1,3])
    Concomitant Agent, Unit of Measure
    Item
    Units
    text
    C2347852 (UMLS CUI [1,1])
    C1519795 (UMLS CUI [1,2])
    C0178602 (UMLS CUI [1,3])
    Concomitant Agent, Frequencies
    Item
    Frequency
    text
    C2347852 (UMLS CUI [1,1])
    C0439603 (UMLS CUI [1,2])
    Concomitant Agent, Drug Administration Routes
    Item
    Route
    text
    C2347852 (UMLS CUI [1,1])
    C0013153 (UMLS CUI [1,2])
    Concomitant Agent, Reason and justification
    Item
    Reason for Medication
    text
    C2347852 (UMLS CUI [1,1])
    C0566251 (UMLS CUI [1,2])
    Concomitant Agent, Start Date, Start time
    Item
    Start Date and Time
    datetime
    C2347852 (UMLS CUI [1,1])
    C0808070 (UMLS CUI [1,2])
    C1301880 (UMLS CUI [1,3])
    Concomitant Medication Previous Occurrence
    Item
    Taken Prior to Study?
    boolean
    C2826667 (UMLS CUI [1])
    Concomitant Medication Ongoing
    Item
    Ongoing?
    boolean
    C2826666 (UMLS CUI [1])
    Concomitant Agent, End Date, End time
    Item
    No, specify End Date and Time
    datetime
    C2347852 (UMLS CUI [1,1])
    C0806020 (UMLS CUI [1,2])
    C1522314 (UMLS CUI [1,3])
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