0 Avaliações

ID

25886

Descrição

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.

Palavras-chave

  1. 25.09.17 25.09.17 -
Titular dos direitos

Glaxo Smith Kline

Transferido a

25. September 2017

DOI

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Licença

Creative Commons BY-NC 3.0

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    GSK AVA100193 Rosiglitazone in Alzheimer´s Disease - Pharmacogenetic and Pharmacogenomic Research

    Pharmacogenetic and Pharmacogenomic Research

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

    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?
    Descrição

    Informed Consent

    Tipo de dados

    boolean

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

    Date informed consent obtained

    Tipo de dados

    date

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

    reason informed consent not obtained

    Tipo de dados

    integer

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

    reason informed consent not obtained

    Tipo de dados

    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?
    Descrição

    Blood sample collection

    Tipo de dados

    boolean

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

    Blood sample collection date

    Tipo de dados

    date

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    Has subject withdrawn consent for PGx-Pharmacogenetic/PGm-Transcriptomic/PGm-Proteomic research?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

    Withdrawal of Consent

    Tipo de dados

    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?
    Descrição

    Blood sample destruction

    Tipo de dados

    boolean

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

    Blood sample destruction reason

    Tipo de dados

    text

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

    Other reason for sample destruction

    Tipo de dados

    text

    Alias
    UMLS CUI [1,1]
    C1948029
    UMLS CUI [1,2]
    C0178913
    UMLS CUI [1,3]
    C3845569

    Similar models

    Pharmacogenetic and Pharmacogenomic Research

    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de dados
    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])
    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])
    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])

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