0 Bedömningar
ID

17492

Beskrivning

NCT00428090 / GSK-AVA105640 A 24-week, double-blind, double-dummy, randomized, parallel-group study to investigate the effects of rosiglitazone (extended release tablets), donepezil, and placebo as monotherapy on cognition and overall clinical response in APOE e4-stratified subjects with mild to moderate Alzheimer’s disease. (REFLECT-1)

Nyckelord

Versioner (2)
  1. 2016-09-18 2016-09-18 -
  2. 2016-09-25 2016-09-25 -
Uppladdad den

18 september 2016

DOI

För en begäran logga in.

Licens

Creative Commons BY-NC-ND 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 Concomitant Medication NCT00428090

    Engelsk

    GSK Concomitant Medication NCT00428090

    1 Formulär  
    Patient Information
    Beskrivning

    Patient Information

    Alias
    UMLS CUI-1
    C1955348
    Subject Identifier
    Beskrivning

    Patient Study ID

    Datatyp

    text

    Alias
    UMLS CUI [1]
    C2348585
    Concomitant Medication
    Beskrivning

    Concomitant Medication

    Alias
    UMLS CUI-1
    C2347852
    Where any concomitant medications taken by the subject during the study?
    Beskrivning

    Concomitant Medications

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C2347852
    Drug Name (Trade Name preferred) (e.g. Aspirin) If "YES", record each medication on a seperate line using Trade Names where possible. If the medication is related to an Adverse Event or Serious Adverse Event, details should be expressed using the same terminology.
    Beskrivning

    Drug Name

    Datatyp

    text

    Alias
    UMLS CUI [1]
    C0013227
    Total Daily Dose (e.g. 400) If "YES", record each medication on a seperate line using Trade Names where possible. If the medication is related to an Adverse Event or Serious Adverse Event, details should be expressed using the same terminology.
    Beskrivning

    Total Daily Dose

    Datatyp

    text

    Alias
    UMLS CUI [1]
    C2348070
    Units (e.g. mg) If "YES", record each medication on a seperate line using Trade Names where possible. If the medication is related to an Adverse Event or Serious Adverse Event, details should be expressed using the same terminology.
    Beskrivning

    Units

    Datatyp

    text

    Alias
    UMLS CUI [1]
    C1519795
    Route (e.g. PO) If "YES", record each medication on a seperate line using Trade Names where possible. If the medication is related to an Adverse Event or Serious Adverse Event, details should be expressed using the same terminology.
    Beskrivning

    Route

    Datatyp

    text

    Alias
    UMLS CUI [1]
    C0013153
    Reason for Medication (e.g. Headache) If "YES", record each medication on a seperate line using Trade Names where possible. If the medication is related to an Adverse Event or Serious Adverse Event, details should be expressed using the same terminology.
    Beskrivning

    Reason for Medication

    Datatyp

    text

    Alias
    UMLS CUI [1,1]
    C0392360
    UMLS CUI [1,2]
    C0013227
    Start Date (Day Month Year) (e.g. 31 MAY 02) If "YES", record each medication on a seperate line using Trade Names where possible. If the medication is related to an Adverse Event or Serious Adverse Event, details should be expressed using the same terminology.
    Beskrivning

    Start date

    Datatyp

    date

    Måttenheter
    • dd/MMM/yy
    Alias
    UMLS CUI [1]
    C0013227
    dd/MMM/yy
    Stop Date (Day Month Year) (e.g. 31 MAY 02) If "YES", record each medication on a seperate line using Trade Names where possible. If the medication is related to an Adverse Event or Serious Adverse Event, details should be expressed using the same terminology.
    Beskrivning

    Stop Date

    Datatyp

    date

    Alias
    UMLS CUI [1]
    C0806020
    Ongoing Medication (Yes - No) If "YES", record each medication on a seperate line using Trade Names where possible. If the medication is related to an Adverse Event or Serious Adverse Event, details should be expressed using the same terminology.
    Beskrivning

    Ongoing Medication

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C2826666
    Tillbaka till toppen

    Similar models

    GSK Concomitant Medication NCT00428090

    1 Formulär
    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datatyp
    Alias
    Item Group
    Patient Information
    C1955348 (UMLS CUI-1)
    Patient Study ID
    Item
    Subject Identifier
    text
    C2348585 (UMLS CUI [1])
    Item Group
    Concomitant Medication
    C2347852 (UMLS CUI-1)
    Concomitant Medications
    Item
    Where any concomitant medications taken by the subject during the study?
    boolean
    C2347852 (UMLS CUI [1])
    Drug Name
    Item
    Drug Name (Trade Name preferred) (e.g. Aspirin) If "YES", record each medication on a seperate line using Trade Names where possible. If the medication is related to an Adverse Event or Serious Adverse Event, details should be expressed using the same terminology.
    text
    C0013227 (UMLS CUI [1])
    Total Daily Dose
    Item
    Total Daily Dose (e.g. 400) If "YES", record each medication on a seperate line using Trade Names where possible. If the medication is related to an Adverse Event or Serious Adverse Event, details should be expressed using the same terminology.
    text
    C2348070 (UMLS CUI [1])
    Units
    Item
    Units (e.g. mg) If "YES", record each medication on a seperate line using Trade Names where possible. If the medication is related to an Adverse Event or Serious Adverse Event, details should be expressed using the same terminology.
    text
    C1519795 (UMLS CUI [1])
    Route
    Item
    Route (e.g. PO) If "YES", record each medication on a seperate line using Trade Names where possible. If the medication is related to an Adverse Event or Serious Adverse Event, details should be expressed using the same terminology.
    text
    C0013153 (UMLS CUI [1])
    Reason for Medication
    Item
    Reason for Medication (e.g. Headache) If "YES", record each medication on a seperate line using Trade Names where possible. If the medication is related to an Adverse Event or Serious Adverse Event, details should be expressed using the same terminology.
    text
    C0392360 (UMLS CUI [1,1])
    C0013227 (UMLS CUI [1,2])
    Start date
    Item
    Start Date (Day Month Year) (e.g. 31 MAY 02) If "YES", record each medication on a seperate line using Trade Names where possible. If the medication is related to an Adverse Event or Serious Adverse Event, details should be expressed using the same terminology.
    date
    C0013227 (UMLS CUI [1])
    Stop Date
    Item
    Stop Date (Day Month Year) (e.g. 31 MAY 02) If "YES", record each medication on a seperate line using Trade Names where possible. If the medication is related to an Adverse Event or Serious Adverse Event, details should be expressed using the same terminology.
    date
    C0806020 (UMLS CUI [1])
    Ongoing Medication
    Item
    Ongoing Medication (Yes - No) If "YES", record each medication on a seperate line using Trade Names where possible. If the medication is related to an Adverse Event or Serious Adverse Event, details should be expressed using the same terminology.
    boolean
    C2826666 (UMLS CUI [1])
    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