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ID

30158

Description

Study ID: 108414 Clinical Study ID: DBU108414 Study Title: TXA107979: A placebo-controlled, single blind, randomized two part study to investigate the tolerability, pharmacokinetics, and brainDopamine D3 receptor occupancy of increasing repeat doses ofGSK618334 for up to 21 days in healthy volunteers. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01036061 https://clinicaltrials.gov/ct2/show/NCT01036061 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: GSK618334 Study Indication: Substance Dependence Documentation part: Telemetry

Lien

https://clinicaltrials.gov/ct2/show/NCT01036061

Mots-clés

  1. 16/05/2018 16/05/2018 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

16 mai 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

Modèle Commentaires :

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    Tolerability, pharmacokinetics, and brain Dopamine D3 receptor occupancy of increasing repeat doses of GSK618334 in healthy adults NCT01036061

    1. StudyEvent: ODM
      1. Telemetry
    Telemetry
    Description

    Telemetry

    Alias
    UMLS CUI-1
    C0039451
    Start Date Telemetry
    Description

    Start Date Telemetry

    Type de données

    date

    Alias
    UMLS CUI [1,1]
    C0039451
    UMLS CUI [1,2]
    C0808070
    Start Time Telemetry
    Description

    Start Time Telemetry

    Type de données

    time

    Alias
    UMLS CUI [1,1]
    C0039451
    UMLS CUI [1,2]
    C1301880
    Stop Date Telemetry
    Description

    Stop Date Telemetry

    Type de données

    date

    Alias
    UMLS CUI [1,1]
    C0039451
    UMLS CUI [1,2]
    C0806020
    Stop Time Telemetry
    Description

    Stop Time Telemetry

    Type de données

    time

    Alias
    UMLS CUI [1]
    C1522314
    Result of Telemetry
    Description

    Result of Telemetry

    Type de données

    integer

    Alias
    UMLS CUI [1,1]
    C0039451
    UMLS CUI [1,2]
    C0438154

    Similar models

    Telemetry

    1. StudyEvent: ODM
      1. Telemetry
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    Telemetry
    C0039451 (UMLS CUI-1)
    Start Date Telemetry
    Item
    Start Date Telemetry
    date
    C0039451 (UMLS CUI [1,1])
    C0808070 (UMLS CUI [1,2])
    Start Time Telemetry
    Item
    Start Time Telemetry
    time
    C0039451 (UMLS CUI [1,1])
    C1301880 (UMLS CUI [1,2])
    Stop Date Telemetry
    Item
    Stop Date Telemetry
    date
    C0039451 (UMLS CUI [1,1])
    C0806020 (UMLS CUI [1,2])
    Stop Time Telemetry
    Item
    Stop Time Telemetry
    time
    C1522314 (UMLS CUI [1])
    Item
    Result of Telemetry
    integer
    C0039451 (UMLS CUI [1,1])
    C0438154 (UMLS CUI [1,2])
    Code List
    Result of Telemetry
    CL Item
    Normal (1)
    CL Item
    Abnormal, Not clinically significant (2)
    CL Item
    Abnormal, Clinically significant (3)

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