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ID

26837

Beschrijving

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

Trefwoorden

  1. 23-10-17 23-10-17 -
  2. 25-10-17 25-10-17 - Julian Varghese
Houder van rechten

GSK

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25 oktober 2017

DOI

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Licentie

Creative Commons BY-NC 3.0

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

    Session 1 +1.58hrs

    1. StudyEvent: ODM
      1. Session 1 +1.58hrs
    Default Itemgroup
    Beschrijving

    Default Itemgroup

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

    Subject number

    Datatype

    text

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

    Visit Date | Visit Time

    Datatype

    datetime

    Alias
    UMLS CUI [1]
    C1320303 (Date of visit)
    SNOMED
    406543005
    UMLS CUI [2]
    C1320304 (Time of visit)
    SNOMED
    406544004
    Panic Symptom List
    Beschrijving

    Panic Symptom List

    Alias
    UMLS CUI-1
    C2945698 (panic symptoms)
    UMLS CUI-2
    C0745732 (List)
    LOINC
    LP204165-7
    This section contained Clinical Outcome Assessment data collection questionnaires or indices, which are protected by copyright laws and therefore have been excluded.
    Beschrijving

    Copyright

    Datatype

    text

    Visual Analog Scale for Anxiety
    Beschrijving

    Visual Analog Scale for Anxiety

    Alias
    UMLS CUI-1
    C3536884 (Visual Analog Scale)
    SNOMED
    273903006
    UMLS CUI-2
    C0003467 (Anxiety)
    SNOMED
    48694002
    LOINC
    MTHU013060
    What is your degree of anxiety?
    Beschrijving

    Anxiety Score

    Datatype

    text

    Alias
    UMLS CUI [1]
    C3483978 (Anxiety score)
    LOINC
    LP150148-7
    Visual Analog Scale for Anxiety
    Beschrijving

    Visual Analog Scale for Anxiety

    Alias
    UMLS CUI-1
    C3536884 (Visual Analog Scale)
    SNOMED
    273903006
    UMLS CUI-2
    C0003467 (Anxiety)
    SNOMED
    48694002
    LOINC
    MTHU013060
    Anxiety Score
    Beschrijving

    Anxiety Score

    Datatype

    float

    Alias
    UMLS CUI [1]
    C3483978 (Anxiety score)
    LOINC
    LP150148-7

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    Session 1 +1.58hrs

    1. StudyEvent: ODM
      1. Session 1 +1.58hrs
    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    Default Itemgroup
    C1320722 (UMLS CUI-1)
    Subject number
    Item
    Subject number
    text
    C2348585 (UMLS CUI [1])
    Visit Date | Visit Time
    Item
    datetime
    C1320303 (UMLS CUI [1])
    C1320304 (UMLS CUI [2])
    Item Group
    C2945698 (UMLS CUI-1)
    C0745732 (UMLS CUI-2)
    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
    C3536884 (UMLS CUI-1)
    C0003467 (UMLS CUI-2)
    Anxiety Score
    Item
    What is your degree of anxiety?
    text
    C3483978 (UMLS CUI [1])
    Item Group
    C3536884 (UMLS CUI-1)
    C0003467 (UMLS CUI-2)
    Anxiety Score
    Item
    float
    C3483978 (UMLS CUI [1])

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