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38277

Beschreibung

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

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Versionen (2)
  1. 06.10.19 06.10.19 -
  2. 24.10.19 24.10.19 -
Rechteinhaber

GlaxoSmithKline

Hochgeladen am

6. Oktober 2019

DOI

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

    Englisch

    Common CRF: Concomitant Medications

    1 Formulare  
    Administrative Data
    Beschreibung

    Administrative Data

    Alias
    UMLS CUI-1
    C1320722
    Site
    Beschreibung

    Study Site

    Datentyp

    text

    Alias
    UMLS CUI [1]
    C2825164
    Patient
    Beschreibung

    Patient name

    Datentyp

    text

    Alias
    UMLS CUI [1]
    C1299487
    Patient No
    Beschreibung

    Patients, Identification number

    Datentyp

    integer

    Alias
    UMLS CUI [1,1]
    C0030705
    UMLS CUI [1,2]
    C1300638
    Concomitant Medications
    Beschreibung

    Concomitant Medications

    Alias
    UMLS CUI-1
    C2347852
    Were any medications recorded on the In-Clinic Medications Taken Diary?
    Beschreibung

    Concomitant Agent

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C2347852
    Sequence Number
    Beschreibung

    Concomitant Agent, Sequence Number

    Datentyp

    integer

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C2348184
    Drug Name (Trade Name preferred)
    Beschreibung

    Concomitant Agent, Medication name

    Datentyp

    text

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

    Concomitant Agent, Medication name, Reported Term

    Datentyp

    text

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C2360065
    UMLS CUI [1,3]
    C2826302
    GSK Drug synonym
    Beschreibung

    Concomitant Agent, Pharmaceutical Preparations, Synonym

    Datentyp

    text

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

    Concomitant Agent, Code

    Datentyp

    text

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0805701
    Failed coding
    Beschreibung

    Concomitant Agent, Code, Failed

    Datentyp

    text

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0805701
    UMLS CUI [1,3]
    C0231175
    Reason for Medication
    Beschreibung

    Concomitant Agent, Indication

    Datentyp

    text

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C3146298
    Start Date
    Beschreibung

    Concomitant Medication Start Date

    Datentyp

    date

    Alias
    UMLS CUI [1]
    C2826734
    Taken Prior to Study?
    Beschreibung

    Concomitant Medication Previous Occurrence

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C2826667
    Ongoing?
    Beschreibung

    Concomitant Medication Ongoing

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C2826666
    No, specify End Date
    Beschreibung

    Concomitant Medication End Date

    Datentyp

    date

    Alias
    UMLS CUI [1]
    C2826744
    Zum Seitenanfang zurückkehren

    Ähnliche Modelle

    Common CRF: Concomitant Medications

    1 Formulare
    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datentyp
    Alias
    Item Group
    Administrative Data
    C1320722 (UMLS CUI-1)
    Study Site
    Item
    Site
    text
    C2825164 (UMLS CUI [1])
    Patient name
    Item
    Patient
    text
    C1299487 (UMLS CUI [1])
    Patients, Identification number
    Item
    Patient No
    integer
    C0030705 (UMLS CUI [1,1])
    C1300638 (UMLS CUI [1,2])
    Item Group
    Concomitant Medications
    C2347852 (UMLS CUI-1)
    Concomitant Agent
    Item
    Were any medications recorded on the In-Clinic Medications Taken Diary?
    boolean
    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 (Trade Name preferred)
    text
    C2347852 (UMLS CUI [1,1])
    C2360065 (UMLS CUI [1,2])
    Concomitant Agent, Medication name, Reported Term
    Item
    Modified reported term
    text
    C2347852 (UMLS CUI [1,1])
    C2360065 (UMLS CUI [1,2])
    C2826302 (UMLS CUI [1,3])
    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, Code
    Item
    GSK Drug Collection code
    text
    C2347852 (UMLS CUI [1,1])
    C0805701 (UMLS CUI [1,2])
    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, Indication
    Item
    Reason for Medication
    text
    C2347852 (UMLS CUI [1,1])
    C3146298 (UMLS CUI [1,2])
    Concomitant Medication Start Date
    Item
    Start Date
    date
    C2826734 (UMLS CUI [1])
    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 Medication End Date
    Item
    No, specify End Date
    date
    C2826744 (UMLS CUI [1])
    Zum Seitenanfang zurückkehren 

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