0 Bedömningar
ID

31486

Beskrivning

Study ID: 104619 Clinical Study ID: 63129 Study Title:A multinational, randomized, double-blind comparison of once daily subcutaneous fondaparinux sodium with placebo for the prevention of venous thromboembolic events in acutely ill medical patients (ARTEMIS). Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: fondaparinux sodium Trade Name: Arixtra Study Indication: Thrombosis, Venous

Nyckelord

Versioner (1)
  1. 28/08/2018 28/08/2018 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

28 août 2018

DOI

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Licens

Creative Commons BY-NC 3.0
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    Subcutaneous fondaparinux sodium for prevention of venous thromboembolic events; Study ID: 104619

    Engelsk

    Medication Record

    1 Formulär  
    1. StudyEvent: ODM
      1. Medication Record
    Meditation Record
    Beskrivning

    Meditation Record

    Alias
    UMLS CUI-1
    C2734539
    Drug Name
    Beskrivning

    Medication Name

    Datatyp

    text

    Alias
    UMLS CUI [1]
    C2360065
    Total Daily Dose/Units
    Beskrivning

    Medication Dose; Daily Dose

    Datatyp

    float

    Alias
    UMLS CUI [1,1]
    C3174092
    UMLS CUI [1,2]
    C2348070
    Route
    Beskrivning

    Drug Administration Routes

    Datatyp

    text

    Alias
    UMLS CUI [1]
    C0013153
    Prior or after?
    Beskrivning

    Drug Administration; Time

    Datatyp

    text

    Alias
    UMLS CUI [1,1]
    C3469597
    UMLS CUI [1,2]
    C0040223
    Duration Dates - Start Date
    Beskrivning

    Pharmaceutical Preparations; Start Date

    Datatyp

    date

    Alias
    UMLS CUI [1,1]
    C0013227
    UMLS CUI [1,2]
    C0808070
    Duration Dates - End Date
    Beskrivning

    Pharmaceutical Preparations; End Date

    Datatyp

    date

    Alias
    UMLS CUI [1,1]
    C0013227
    UMLS CUI [1,2]
    C0806020
    Indication
    Beskrivning

    Pharmaceutical Preparations; Indication

    Datatyp

    text

    Alias
    UMLS CUI [1,1]
    C0013227
    UMLS CUI [1,2]
    C3146298
    A.E. Form Number
    Beskrivning

    Pharmaceutical Preparations; Adverse Event Document Number

    Datatyp

    integer

    Alias
    UMLS CUI [1,1]
    C0013227
    UMLS CUI [1,2]
    C0877248
    UMLS CUI [1,3]
    C1704732
    UMLS CUI [1,4]
    C0237753
    Tillbaka till toppen

    Similar models

    Medication Record

    1 Formulär
    1. StudyEvent: ODM
      1. Medication Record
    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datatyp
    Alias
    Item Group
    Meditation Record
    C2734539 (UMLS CUI-1)
    Medication Name
    Item
    Drug Name
    text
    C2360065 (UMLS CUI [1])
    Medication Dose; Daily Dose
    Item
    Total Daily Dose/Units
    float
    C3174092 (UMLS CUI [1,1])
    C2348070 (UMLS CUI [1,2])
    Drug Administration Routes
    Item
    Route
    text
    C0013153 (UMLS CUI [1])
    Item
    Prior or after?
    text
    C3469597 (UMLS CUI [1,1])
    C0040223 (UMLS CUI [1,2])
    Drug Administration; Time
    Code List
    Prior or after?
    CL Item
    Prior (Prior)
    CL Item
    After (After)
    Pharmaceutical Preparations; Start Date
    Item
    Duration Dates - Start Date
    date
    C0013227 (UMLS CUI [1,1])
    C0808070 (UMLS CUI [1,2])
    Pharmaceutical Preparations; End Date
    Item
    Duration Dates - End Date
    date
    C0013227 (UMLS CUI [1,1])
    C0806020 (UMLS CUI [1,2])
    Pharmaceutical Preparations; Indication
    Item
    Indication
    text
    C0013227 (UMLS CUI [1,1])
    C3146298 (UMLS CUI [1,2])
    Pharmaceutical Preparations; Adverse Event Document Number
    Item
    A.E. Form Number
    integer
    C0013227 (UMLS CUI [1,1])
    C0877248 (UMLS CUI [1,2])
    C1704732 (UMLS CUI [1,3])
    C0237753 (UMLS CUI [1,4])
    Tillbaka till toppen 

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