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

Versões (1)
  1. 25/09/2017 25/09/2017 -
Titular dos direitos

Glaxo Smith Kline

Transferido a

25 de setembro de 2017

DOI

Para um pedido faça login.

Licença

Creative Commons BY-NC 3.0
Comentários do modelo :

Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.

Voltar para os comentários do modelo
Comentários do grupo de itens para :

Comentários do item para :

  • Os mais recentes
  • Os mais antigos
  • Preferidos
  • Os mais recentes
    • Os mais recentes
    • Os mais antigos
    • Preferidos

    Sem comentários

    Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.

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

    Inglês

    Pharmacogenetic and Pharmacogenomic Research

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

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

    Alias
    UMLS CUI-1
    C2347501 (Pharmacogenomic Testing)
    UMLS CUI-2
    C1327760 (Proteomic Profiling)
    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 (Informed Consent)
    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 (Date in time)
    SNOMED
    410671006
    UMLS CUI [1,2]
    C0021430 (Informed Consent)
    If No, check
    Descrição

    reason informed consent not obtained

    Tipo de dados

    integer

    Alias
    UMLS CUI [1,1]
    C0392360 (Indication of (contextual qualifier))
    SNOMED
    230165009
    LOINC
    MTHU008319
    UMLS CUI [1,2]
    C0021430 (Informed Consent)
    UMLS CUI [1,3]
    C1882120 (Not Obtained)
    If other reason please specify
    Descrição

    reason informed consent not obtained

    Tipo de dados

    text

    Alias
    UMLS CUI [1,1]
    C3845569 (Specify Other)
    UMLS CUI [1,2]
    C0021430 (Informed Consent)
    UMLS CUI [1,3]
    C1882120 (Not Obtained)
    Has a blood sample been collected for PGx-pharmacogenetic research?
    Descrição

    Blood sample collection

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0005834 (Collection of blood specimen for laboratory procedure)
    SNOMED
    82078001
    LOINC
    LP125037-4
    If Yes, record the date sample taken
    Descrição

    Blood sample collection date

    Tipo de dados

    date

    Alias
    UMLS CUI [1,1]
    C0005834 (Collection of blood specimen for laboratory procedure)
    SNOMED
    82078001
    LOINC
    LP125037-4
    UMLS CUI [1,2]
    C0011008 (Date in time)
    SNOMED
    410671006
    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 (Consent Withdrawn)
    UMLS CUI [1,2]
    C2347501 (Pharmacogenomic Testing)
    UMLS CUI [1,3]
    C1327760 (Proteomic Profiling)
    Has a request been made for sample destruction?
    Descrição

    Blood sample destruction

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1,1]
    C1948029 (Destruction (action))
    UMLS CUI [1,2]
    C0178913 (Blood specimen)
    SNOMED
    119297000
    If Yes, check one reason
    Descrição

    Blood sample destruction reason

    Tipo de dados

    text

    Alias
    UMLS CUI [1,1]
    C1948029 (Destruction (action))
    UMLS CUI [1,2]
    C0178913 (Blood specimen)
    SNOMED
    119297000
    UMLS CUI [1,3]
    C0392360 (Indication of (contextual qualifier))
    SNOMED
    230165009
    LOINC
    MTHU008319
    Other reason for sample destruction
    Descrição

    Other reason for sample destruction

    Tipo de dados

    text

    Alias
    UMLS CUI [1,1]
    C1948029 (Destruction (action))
    UMLS CUI [1,2]
    C0178913 (Blood specimen)
    SNOMED
    119297000
    UMLS CUI [1,3]
    C3845569 (Specify Other)
    Voltar ao início da página

    Similar models

    Pharmacogenetic and Pharmacogenomic Research

    1 Formulários
    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])
    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])
    Voltar ao início da página 

    Ajuda

    Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

    Watch Tutorial