ID

25886

Beskrivning

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.

Nyckelord

Versioner (1)
  1. 2017-09-25 2017-09-25 -
Rättsinnehavare

Glaxo Smith Kline

Uppladdad den

25 september 2017

DOI

För en begäran logga in.

Licens

Creative Commons BY-NC 3.0
Modellkommentarer :

Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.

Tillbaka till modellkommentarer
Itemgroup-kommentar för :

Item-kommentar för :

  • Senaste
  • Äldsta
  • Önskad
  • Senaste
    • Senaste
    • Äldsta
    • Önskad

    Inga kommentarer

    Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.

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

    Engelsk

    Pharmacogenetic and Pharmacogenomic Research

    1 Formulär  
    PGx-Pharmacogenetic/PGm-Transcriptomic/PGM-Proteomic Research
    Beskrivning

    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?
    Beskrivning

    Informed Consent

    Datatyp

    boolean

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

    Date informed consent obtained

    Datatyp

    date

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

    reason informed consent not obtained

    Datatyp

    integer

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

    reason informed consent not obtained

    Datatyp

    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?
    Beskrivning

    Blood sample collection

    Datatyp

    boolean

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

    Blood sample collection date

    Datatyp

    date

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    Has subject withdrawn consent for PGx-Pharmacogenetic/PGm-Transcriptomic/PGm-Proteomic research?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

    Withdrawal of Consent

    Datatyp

    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?
    Beskrivning

    Blood sample destruction

    Datatyp

    boolean

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

    Blood sample destruction reason

    Datatyp

    text

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

    Other reason for sample destruction

    Datatyp

    text

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

    Similar models

    Pharmacogenetic and Pharmacogenomic Research

    1 Formulär
    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datatyp
    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])
    Tillbaka till toppen 

    Hjälp

    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