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ID

22111

Description

The present pharmacokinetic study is designed to assess the pharmacokinetics of RSG XR as monotherapy in patients with mild Alzheimer's disease (AD) as such information will not be obtained from the current phase III trials . The study aims to enroll fourteen patients (seven of each APOE genotype). Each patient will receive a single oral dose of 4mg of RSG XR in the morning under fasted conditions and PK samples will be taken up to 36h. GSK Source & Descriptions: https://clinicaltrials.gov/ct2/show/NCT00688207?term=NCT00688207&rank=1

Link

https://clinicaltrials.gov/ct2/show/NCT00688207?term=NCT00688207&rank=1

Keywords

Versions (2)
  1. 5/8/17 5/8/17 -
  2. 5/20/17 5/20/17 -
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May 20, 2017

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Creative Commons BY-NC 3.0
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    Concomitant Medications Mild Alzheimer's Disease to Assess the of Extended Release Formulation of Rosiglitazone NCT00688207 / GSK-AVA109941

    English

    Concomitant Medications Mild Alzheimer's Disease to Assess the of Extended Release Formulation of Rosiglitazone NCT00688207 / GSK-AVA109941

    1 forms  
    Concomitant Medication
    Description

    Concomitant Medication

    Alias
    UMLS CUI-1
    C2347852
    Were any concomitant medications taken by the subject during the study? if YES record each medication on a separate line using Trade Names where possible. If yes, record each medication on a separate line using Trade Names where possible.
    Description

    Concomitant Medication

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C2347852
    Medication
    Description

    Medication

    Alias
    UMLS CUI-1
    C0013227
    Drug name (Trade Name preferred) e.g. Aspirin
    Description

    Drug name

    Data type

    text

    Alias
    UMLS CUI [1]
    C0013227
    Unit Dose e.g. 200
    Description

    Unit Dose

    Data type

    float

    Alias
    UMLS CUI [1,1]
    C0869039
    UMLS CUI [1,2]
    C0013227
    Units* (eg. mg)
    Description

    Units

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C1519795
    UMLS CUI [1,2]
    C0013227
    Frequency* (e.g. BID)
    Description

    Frequency

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C3476109
    UMLS CUI [1,2]
    C0013227
    Route* (e.g. PO)
    Description

    Route

    Data type

    text

    Alias
    UMLS CUI [1]
    C0013153
    Reason for Medication (e.g. Headache)
    Description

    Reason for Medication

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0392360
    UMLS CUI [1,2]
    C0013227
    Start Date (e.g. 31 May 03)
    Description

    Start Date

    Data type

    date

    Alias
    UMLS CUI [1,1]
    C0013227
    UMLS CUI [1,2]
    C0808070
    Start time (e.g. 14:10)
    Description

    Start time

    Data type

    time

    Measurement units
    • hh:min
    Alias
    UMLS CUI [1,1]
    C0013227
    UMLS CUI [1,2]
    C1301880
    hh:min
    Taken Prior to Study? (e.g. N)
    Description

    Taken Prior to Study

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C2826667
    Stop Date (e.g. 31 May 03)
    Description

    Stop Date

    Data type

    date

    Alias
    UMLS CUI [1,1]
    C0013227
    UMLS CUI [1,2]
    C0806020
    Stop Time (e.g. 23:00)
    Description

    Stop Time

    Data type

    time

    Alias
    UMLS CUI [1,1]
    C0013227
    UMLS CUI [1,2]
    C1522314
    Ongoing Medication? (e.g. N)
    Description

    Ongoing Medication

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C2826666
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    Similar models

    Concomitant Medications Mild Alzheimer's Disease to Assess the of Extended Release Formulation of Rosiglitazone NCT00688207 / GSK-AVA109941

    1 forms
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    Concomitant Medication
    C2347852 (UMLS CUI-1)
    Concomitant Medication
    Item
    Were any concomitant medications taken by the subject during the study? if YES record each medication on a separate line using Trade Names where possible. If yes, record each medication on a separate line using Trade Names where possible.
    boolean
    C2347852 (UMLS CUI [1])
    Item Group
    Medication
    C0013227 (UMLS CUI-1)
    Drug name
    Item
    Drug name (Trade Name preferred) e.g. Aspirin
    text
    C0013227 (UMLS CUI [1])
    Unit Dose
    Item
    Unit Dose e.g. 200
    float
    C0869039 (UMLS CUI [1,1])
    C0013227 (UMLS CUI [1,2])
    Units
    Item
    Units* (eg. mg)
    text
    C1519795 (UMLS CUI [1,1])
    C0013227 (UMLS CUI [1,2])
    Frequency
    Item
    Frequency* (e.g. BID)
    text
    C3476109 (UMLS CUI [1,1])
    C0013227 (UMLS CUI [1,2])
    Route
    Item
    Route* (e.g. PO)
    text
    C0013153 (UMLS CUI [1])
    Reason for Medication
    Item
    Reason for Medication (e.g. Headache)
    text
    C0392360 (UMLS CUI [1,1])
    C0013227 (UMLS CUI [1,2])
    Start Date
    Item
    Start Date (e.g. 31 May 03)
    date
    C0013227 (UMLS CUI [1,1])
    C0808070 (UMLS CUI [1,2])
    Start time
    Item
    Start time (e.g. 14:10)
    time
    C0013227 (UMLS CUI [1,1])
    C1301880 (UMLS CUI [1,2])
    Taken Prior to Study
    Item
    Taken Prior to Study? (e.g. N)
    boolean
    C2826667 (UMLS CUI [1])
    Stop Date
    Item
    Stop Date (e.g. 31 May 03)
    date
    C0013227 (UMLS CUI [1,1])
    C0806020 (UMLS CUI [1,2])
    Stop Time
    Item
    Stop Time (e.g. 23:00)
    time
    C0013227 (UMLS CUI [1,1])
    C1522314 (UMLS CUI [1,2])
    Ongoing Medication
    Item
    Ongoing Medication? (e.g. N)
    boolean
    C2826666 (UMLS CUI [1])
    Back to the top of the page 

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