0 Bedömningar
ID

39293

Beskrivning

Study ID: 110771 Clinical Study ID: 110771 Study Title: An open label positron emission tomography (PET) study to investigate brain penetration by [carbonyl-11C] GSK1034702 in healthy subjects 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: Positron Emission Tomography Trade Name: Carbonyl-11C Study Indication: Cognitive Disorders, Alzheimer's disease, schizophrenia.

Nyckelord

Versioner (1)
  1. 2019-12-17 2019-12-17 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

17 december 2019

DOI

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Licens

Creative Commons BY-NC 3.0
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    Brain Penetration by [Carbonyl-11C] GSK1034702; 110771

    Engelsk

    Liver Events Assessment

    1 Formulär  
    Administrative Data
    Beskrivning

    Administrative Data

    Alias
    UMLS CUI-1
    C1320722
    Subject Identifier
    Beskrivning

    Clinical Trial Subject Unique Identifier

    Datatyp

    integer

    Alias
    UMLS CUI [1]
    C2348585
    Liver Events Assessment
    Beskrivning

    Liver Events Assessment

    Alias
    UMLS CUI-1
    C0023884
    UMLS CUI-2
    C0877248
    UMLS CUI-3
    C0220825
    Was there any protocol defined liver chemistry event for the lab samples collected at this visit?
    Beskrivning

    Liver, Chemistry, Clinical, Adverse Event

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0023884
    UMLS CUI [1,2]
    C0008000
    UMLS CUI [1,3]
    C0877248
    If Yes, which type of liver chemistry event?
    Beskrivning

    Liver, Chemistry, Clinical, Adverse Event, Type

    Datatyp

    text

    Alias
    UMLS CUI [1,1]
    C0023884
    UMLS CUI [1,2]
    C0008000
    UMLS CUI [1,3]
    C0877248
    UMLS CUI [1,4]
    C0332307
    Tillbaka till toppen

    Similar models

    Liver Events Assessment

    1 Formulär
    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datatyp
    Alias
    Item Group
    Administrative Data
    C1320722 (UMLS CUI-1)
    Clinical Trial Subject Unique Identifier
    Item
    Subject Identifier
    integer
    C2348585 (UMLS CUI [1])
    Item Group
    Liver Events Assessment
    C0023884 (UMLS CUI-1)
    C0877248 (UMLS CUI-2)
    C0220825 (UMLS CUI-3)
    Liver, Chemistry, Clinical, Adverse Event
    Item
    Was there any protocol defined liver chemistry event for the lab samples collected at this visit?
    boolean
    C0023884 (UMLS CUI [1,1])
    C0008000 (UMLS CUI [1,2])
    C0877248 (UMLS CUI [1,3])
    Item
    If Yes, which type of liver chemistry event?
    text
    C0023884 (UMLS CUI [1,1])
    C0008000 (UMLS CUI [1,2])
    C0877248 (UMLS CUI [1,3])
    C0332307 (UMLS CUI [1,4])
    Liver, Chemistry, Clinical, Adverse Event, Type
    Code List
    If Yes, which type of liver chemistry event?
    CL Item
    Liver Event Monitoring Criteria (subject has met protocol defined liver chemistry MONITORING criteria). (1)
    CL Item
    Liver Event Stopping Criteria (subject has met protocol defined liver chemistry STOPPING criteria or has been monitored for the protocol specific time period and continues to meet liver chemistry event criteria). (2)
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