0 Beoordelingen
ID

38094

Beschrijving

Study ID: 105036 Clinical Study ID: 105036 Study Title: A single-blind, randomized, placebo-controlled study to investigate the safety, tolerability, and potential effects on betamethasone pharmacokinetics of a co-administered infusion of GSK221149A in healthy female subjects Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: N/A Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: betamethasone Trade Name: Retosiban Study Indication: Women's Health & Pregnancy - Other, pre-term labour

Trefwoorden

Versies (1)
  1. 17-09-19 17-09-19 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

17 september 2019

DOI

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Licentie

Creative Commons BY-NC 3.0
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    Betamethasone pharmacokinetics of a co-administered infusion of GSK221149A; 105036

    Engels

    PGx - Pharmacogenetic Research Consent

    1 Formulieren  
    PGx-Pharmcogenetic Research Consent
    Beschrijving

    PGx-Pharmcogenetic Research Consent

    Alias
    UMLS CUI-1
    C2347500
    UMLS CUI-2
    C0021430
    Has informed consent been obtained for PGx-Pharmacogenetic research?
    Beschrijving

    Pharmacogenetic Test, Informed Consent

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C2347500
    UMLS CUI [1,2]
    C0021430
    If Yes, record: Date informed consent obtained for PGx-Pharmacogenetic research
    Beschrijving

    Pharmacogenetic Test, Informed Consent, Date in time

    Datatype

    date

    Alias
    UMLS CUI [1,1]
    C2347500
    UMLS CUI [1,2]
    C0021430
    UMLS CUI [1,3]
    C0011008
    If Yes, Has a blood sample been collected for PGx-pharmacogenetic (DNA) research?
    Beschrijving

    Pharmacogenetic Test, Collection of blood specimen for laboratory procedure

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C2347500
    UMLS CUI [1,2]
    C0005834
    If Yes, record date sample taken
    Beschrijving

    Pharmacogenetic Test, Collection of blood specimen for laboratory procedure, Date in time

    Datatype

    date

    Alias
    UMLS CUI [1,1]
    C2347500
    UMLS CUI [1,2]
    C0005834
    UMLS CUI [1,3]
    C0011008
    If No (informed consent), check reason
    Beschrijving

    Pharmacogenetic Test, Informed Consent, Reason and justification

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C2347500
    UMLS CUI [1,2]
    C0021430
    UMLS CUI [1,3]
    C0566251
    Terug naar het begin van de pagina

    Similar models

    PGx - Pharmacogenetic Research Consent

    1 Formulieren
    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    PGx-Pharmcogenetic Research Consent
    C2347500 (UMLS CUI-1)
    C0021430 (UMLS CUI-2)
    Pharmacogenetic Test, Informed Consent
    Item
    Has informed consent been obtained for PGx-Pharmacogenetic research?
    boolean
    C2347500 (UMLS CUI [1,1])
    C0021430 (UMLS CUI [1,2])
    Pharmacogenetic Test, Informed Consent, Date in time
    Item
    If Yes, record: Date informed consent obtained for PGx-Pharmacogenetic research
    date
    C2347500 (UMLS CUI [1,1])
    C0021430 (UMLS CUI [1,2])
    C0011008 (UMLS CUI [1,3])
    Pharmacogenetic Test, Collection of blood specimen for laboratory procedure
    Item
    If Yes, Has a blood sample been collected for PGx-pharmacogenetic (DNA) research?
    boolean
    C2347500 (UMLS CUI [1,1])
    C0005834 (UMLS CUI [1,2])
    Pharmacogenetic Test, Collection of blood specimen for laboratory procedure, Date in time
    Item
    If Yes, record date sample taken
    date
    C2347500 (UMLS CUI [1,1])
    C0005834 (UMLS CUI [1,2])
    C0011008 (UMLS CUI [1,3])
    Item
    If No (informed consent), check reason
    text
    C2347500 (UMLS CUI [1,1])
    C0021430 (UMLS CUI [1,2])
    C0566251 (UMLS CUI [1,3])
    Pharmacogenetic Test, Informed Consent, Reason and justification
    Code List
    If No (informed consent), check reason
    CL Item
    Subject declined (1)
    CL Item
    Subject not asked by Investigator (2)
    CL Item
    Other, specify (3)
    Terug naar het begin van de pagina 

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