0 Evaluaciones

ID

26526

Descripción

Study ID: 100690 Clinical Study ID: NKP100690 Study Title: A randomised, double blind triple dummy, placebo controlled balanced incomplete block crossover study to evaluate the change in response to a 7% CO2 challenge and pharmacokinetics of single oral doses of GW597599 and paroxetine (5 or 7.5 mg) either alone or in combination, or alprazolam (0.75 mg) in healthy volunteers Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 1 Study Recruitment Status: Completed Generic Name: paroxetine Trade Name: Tagonis,Seroxat,Paxil,Paroxat,Deroxat,Aropax Study Indication: Depressive Disorder and Anxiety Disorders CRF Seiten: 255-365

Palabras clave

  1. 18/10/17 18/10/17 -
Titular de derechos de autor

GSK

Subido en

18 de octubre de 2017

DOI

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Licencia

Creative Commons BY-NC 3.0

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    7% CO2, GW597599, paroxetine andor alprazolam in healthy volunteers 100690

    Screening; Surveys and Questionnaires

    Default Itemgroup
    Descripción

    Default Itemgroup

    Alias
    UMLS CUI-1
    C1320722
    Subject number
    Descripción

    Subject number

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C2348585
    Visit Date & Time
    Descripción

    Visit Date Time

    Tipo de datos

    datetime

    Alias
    UMLS CUI [1,1]
    C1320303
    UMLS CUI [1,2]
    C1320304
    Surveys and Questionnaires
    Descripción

    Surveys and Questionnaires

    Alias
    UMLS CUI-1
    C4042892
    Body Sensations Questionnaire (BSQ)
    Descripción

    Body Sensations Questionnaire (BSQ)

    Alias
    UMLS CUI-1
    C0242821
    UMLS CUI-2
    C1455667
    UMLS CUI-3
    C0034394
    This section contained Clinical Outcome Assessment data collection questionnaires or indices, which are protected by copyright laws and therefore have been excluded.
    Descripción

    Copyright

    Tipo de datos

    text

    Anxiety Sensitivity Index (ASI)
    Descripción

    Anxiety Sensitivity Index (ASI)

    Alias
    UMLS CUI-1
    C0003467
    UMLS CUI-2
    C1522640
    UMLS CUI-3
    C0918012
    This section contained Clinical Outcome Assessment data collection questionnaires or indices, which are protected by copyright laws and therefore have been excluded.
    Descripción

    Copyright

    Tipo de datos

    text

    Similar models

    Screening; Surveys and Questionnaires

    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    Alias
    Item Group
    Default Itemgroup
    C1320722 (UMLS CUI-1)
    Subject number
    Item
    Subject number
    text
    C2348585 (UMLS CUI [1])
    Visit Date Time
    Item
    Visit Date & Time
    datetime
    C1320303 (UMLS CUI [1,1])
    C1320304 (UMLS CUI [1,2])
    Item Group
    Surveys and Questionnaires
    C4042892 (UMLS CUI-1)
    Item Group
    Body Sensations Questionnaire (BSQ)
    C0242821 (UMLS CUI-1)
    C1455667 (UMLS CUI-2)
    C0034394 (UMLS CUI-3)
    Copyright
    Item
    This section contained Clinical Outcome Assessment data collection questionnaires or indices, which are protected by copyright laws and therefore have been excluded.
    text
    Item Group
    Anxiety Sensitivity Index (ASI)
    C0003467 (UMLS CUI-1)
    C1522640 (UMLS CUI-2)
    C0918012 (UMLS CUI-3)
    Copyright
    Item
    This section contained Clinical Outcome Assessment data collection questionnaires or indices, which are protected by copyright laws and therefore have been excluded.
    text

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