ID

25886

Beschrijving

A 24 week double-blind, randomised, placebo-controlled, parallel-group dose-ranging study to investigate the effects of rosiglitazone (extended release tablets) on cognition in subjects with mild to moderate Alzheimer's disease.

Trefwoorden

Versies (1)
  1. 25-09-17 25-09-17 -
Houder van rechten

Glaxo Smith Kline

Geüploaded op

25 september 2017

DOI

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Licentie

Creative Commons BY-NC 3.0
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    GSK AVA100193 Rosiglitazone in Alzheimer´s Disease - Pharmacogenetic and Pharmacogenomic Research

    Engels

    Pharmacogenetic and Pharmacogenomic Research

    1 Formulieren  
    PGx-Pharmacogenetic/PGm-Transcriptomic/PGM-Proteomic Research
    Beschrijving

    PGx-Pharmacogenetic/PGm-Transcriptomic/PGM-Proteomic Research

    Alias
    UMLS CUI-1
    C2347501
    UMLS CUI-2
    C1327760
    Has informed consent been obtained for PGx-Pharmacogenetic/PGm-Transcriptomic/PGm-Proteomic Research?
    Beschrijving

    Informed Consent

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0021430
    If Yes, record the date informed consent obtained for PGxPharmacogenetic/PGm-Transcriptomic/PGm-Proteomic research
    Beschrijving

    Date informed consent obtained

    Datatype

    date

    Alias
    UMLS CUI [1,1]
    C0011008
    UMLS CUI [1,2]
    C0021430
    If No, check
    Beschrijving

    reason informed consent not obtained

    Datatype

    integer

    Alias
    UMLS CUI [1,1]
    C0392360
    UMLS CUI [1,2]
    C0021430
    UMLS CUI [1,3]
    C1882120
    If other reason please specify
    Beschrijving

    reason informed consent not obtained

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C3845569
    UMLS CUI [1,2]
    C0021430
    UMLS CUI [1,3]
    C1882120
    Has a blood sample been collected for PGx-pharmacogenetic research?
    Beschrijving

    Blood sample collection

    Datatype

    boolean

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

    Blood sample collection date

    Datatype

    date

    Alias
    UMLS CUI [1,1]
    C0005834
    UMLS CUI [1,2]
    C0011008
    Has subject withdrawn consent for PGx-Pharmacogenetic/PGm-Transcriptomic/PGm-Proteomic research?
    Beschrijving

    Withdrawal of Consent

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C1707492
    UMLS CUI [1,2]
    C2347501
    UMLS CUI [1,3]
    C1327760
    Has a request been made for sample destruction?
    Beschrijving

    Blood sample destruction

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C1948029
    UMLS CUI [1,2]
    C0178913
    If Yes, check one reason
    Beschrijving

    Blood sample destruction reason

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C1948029
    UMLS CUI [1,2]
    C0178913
    UMLS CUI [1,3]
    C0392360
    Other reason for sample destruction
    Beschrijving

    Other reason for sample destruction

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C1948029
    UMLS CUI [1,2]
    C0178913
    UMLS CUI [1,3]
    C3845569
    Terug naar het begin van de pagina

    Similar models

    Pharmacogenetic and Pharmacogenomic Research

    1 Formulieren
    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    PGx-Pharmacogenetic/PGm-Transcriptomic/PGM-Proteomic Research
    C2347501 (UMLS CUI-1)
    C1327760 (UMLS CUI-2)
    Informed Consent
    Item
    Has informed consent been obtained for PGx-Pharmacogenetic/PGm-Transcriptomic/PGm-Proteomic Research?
    boolean
    C0021430 (UMLS CUI [1])
    Date informed consent obtained
    Item
    If Yes, record the date informed consent obtained for PGxPharmacogenetic/PGm-Transcriptomic/PGm-Proteomic research
    date
    C0011008 (UMLS CUI [1,1])
    C0021430 (UMLS CUI [1,2])
    Item
    If No, check
    integer
    C0392360 (UMLS CUI [1,1])
    C0021430 (UMLS CUI [1,2])
    C1882120 (UMLS CUI [1,3])
    reason informed consent not obtained
    Code List
    If No, check
    CL Item
    Subject declined (1)
    CL Item
    Subject not asked by Investigator (2)
    CL Item
    Other (3)
    reason informed consent not obtained
    Item
    If other reason please specify
    text
    C3845569 (UMLS CUI [1,1])
    C0021430 (UMLS CUI [1,2])
    C1882120 (UMLS CUI [1,3])
    Blood sample collection
    Item
    Has a blood sample been collected for PGx-pharmacogenetic research?
    boolean
    C0005834 (UMLS CUI [1])
    Blood sample collection date
    Item
    If Yes, record the date sample taken
    date
    C0005834 (UMLS CUI [1,1])
    C0011008 (UMLS CUI [1,2])
    Withdrawal of Consent
    Item
    Has subject withdrawn consent for PGx-Pharmacogenetic/PGm-Transcriptomic/PGm-Proteomic research?
    boolean
    C1707492 (UMLS CUI [1,1])
    C2347501 (UMLS CUI [1,2])
    C1327760 (UMLS CUI [1,3])
    Blood sample destruction
    Item
    Has a request been made for sample destruction?
    boolean
    C1948029 (UMLS CUI [1,1])
    C0178913 (UMLS CUI [1,2])
    Item
    If Yes, check one reason
    text
    C1948029 (UMLS CUI [1,1])
    C0178913 (UMLS CUI [1,2])
    C0392360 (UMLS CUI [1,3])
    Blood sample destruction reason
    Code List
    If Yes, check one reason
    CL Item
    Subject requested (1)
    CL Item
    Other (Z)
    Other reason for sample destruction
    Item
    Other reason for sample destruction
    text
    C1948029 (UMLS CUI [1,1])
    C0178913 (UMLS CUI [1,2])
    C3845569 (UMLS CUI [1,3])
    Terug naar het begin van de pagina 

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