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26526

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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

Nyckelord

Versioner (1)
  1. 2017-10-18 2017-10-18 -
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GSK

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18 oktober 2017

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Creative Commons BY-NC 3.0
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    7% CO2, GW597599, paroxetine andor alprazolam in healthy volunteers 100690

    Engelsk

    Screening; Surveys and Questionnaires

    1 Formulär  
    Default Itemgroup
    Beskrivning

    Default Itemgroup

    Alias
    UMLS CUI-1
    C1320722 (Administrative documentation)
    SNOMED
    405624007
    Subject number
    Beskrivning

    Subject number

    Datatyp

    text

    Alias
    UMLS CUI [1]
    C2348585 (Clinical Trial Subject Unique Identifier)
    Visit Date & Time
    Beskrivning

    Visit Date Time

    Datatyp

    datetime

    Alias
    UMLS CUI [1,1]
    C1320303 (Date of visit)
    SNOMED
    406543005
    UMLS CUI [1,2]
    C1320304 (Time of visit)
    SNOMED
    406544004
    Surveys and Questionnaires
    Beskrivning

    Surveys and Questionnaires

    Alias
    UMLS CUI-1
    C4042892 (Surveys and Questionnaires)
    Body Sensations Questionnaire (BSQ)
    Beskrivning

    Body Sensations Questionnaire (BSQ)

    Alias
    UMLS CUI-1
    C0242821 (Human body)
    UMLS CUI-2
    C1455667 (Sensation quality)
    SNOMED
    272144002
    UMLS CUI-3
    C0034394 (Questionnaires)
    This section contained Clinical Outcome Assessment data collection questionnaires or indices, which are protected by copyright laws and therefore have been excluded.
    Beskrivning

    Copyright

    Datatyp

    text

    Anxiety Sensitivity Index (ASI)
    Beskrivning

    Anxiety Sensitivity Index (ASI)

    Alias
    UMLS CUI-1
    C0003467 (Anxiety)
    SNOMED
    48694002
    LOINC
    MTHU013060
    UMLS CUI-2
    C1522640 (stimulus sensitivity)
    UMLS CUI-3
    C0918012 (Index)
    This section contained Clinical Outcome Assessment data collection questionnaires or indices, which are protected by copyright laws and therefore have been excluded.
    Beskrivning

    Copyright

    Datatyp

    text

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    Similar models

    Screening; Surveys and Questionnaires

    1 Formulär
    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datatyp
    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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