0 Evaluaciones

ID

22172

Descripción

This is an open-label extension to study 49653/461, to assess the long-term safety of rosiglitazone (extended release tablets) in subjects with mild to moderate Alzheimer's Disease. GSK Source & Descriptions: https://clinicaltrials.gov/ct2/show/NCT00381238?term=NCT00381238&rank=1

Link

https://clinicaltrials.gov/ct2/show/NCT00381238?term=NCT00381238&rank=1

Palabras clave

  1. 9/5/17 9/5/17 -
  2. 22/5/17 22/5/17 -
Subido en

22 de mayo de 2017

DOI

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Licencia

Creative Commons BY-NC 3.0

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    Concomitant Medications Open-Label Extension Assessing Long-Term Safety Of Rosiglitazone In Subjects With Mild To Moderate Alzheimer's Disease NCT00381238

    Concomitant Medications Open-Label Extension Assessing Long-Term Safety Of Rosiglitazone In Subjects With Mild To Moderate Alzheimer's Disease NCT00381238

    Concomitant Medications
    Descripción

    Concomitant Medications

    Alias
    UMLS CUI-1
    C2347852 (Concomitant Agent)
    Were any concomitant medications taken by the subject prior to screening and/or during the study? If yes, record each medication on a separate line using Trade Names where possible.
    Descripción

    Concomitant Medication

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C2347852 (Concomitant Agent)
    Medication
    Descripción

    Medication

    Alias
    UMLS CUI-1
    C0013227 (Pharmaceutical Preparations)
    SNOMED
    763158003
    LOINC
    LP100609-9
    Drug name (Trade Name preferred) e.g. Aspirin
    Descripción

    Drug name

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C0013227 (Pharmaceutical Preparations)
    SNOMED
    763158003
    LOINC
    LP100609-9
    Unit Dose e.g. 200
    Descripción

    Unit Dose

    Tipo de datos

    float

    Alias
    UMLS CUI [1,1]
    C0013227 (Pharmaceutical Preparations)
    SNOMED
    763158003
    LOINC
    LP100609-9
    UMLS CUI [1,2]
    C0869039 (Unit dose)
    SNOMED
    408102007
    Units* (eg. mg)
    Descripción

    Units

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C0013227 (Pharmaceutical Preparations)
    SNOMED
    763158003
    LOINC
    LP100609-9
    UMLS CUI [1,2]
    C1519795 (Unit of Measure)
    SNOMED
    767524001
    Frequency* (e.g. BID)
    Descripción

    Frequency

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C3476109 (Medication frequency)
    LOINC
    LP149758-7
    Route* (e.g. PO)
    Descripción

    Route

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C0013153 (Drug Administration Routes)
    SNOMED
    410675002
    LOINC
    LP40261-7
    Reason for Medication (e.g. Headache)
    Descripción

    Reason for Medication

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C0013227 (Pharmaceutical Preparations)
    SNOMED
    763158003
    LOINC
    LP100609-9
    UMLS CUI [1,2]
    C0392360 (Indication of (contextual qualifier))
    SNOMED
    230165009
    LOINC
    MTHU008319
    Start Date (e.g. 31 May 03)
    Descripción

    Start Date

    Tipo de datos

    date

    Alias
    UMLS CUI [1,1]
    C0013227 (Pharmaceutical Preparations)
    SNOMED
    763158003
    LOINC
    LP100609-9
    UMLS CUI [1,2]
    C0808070 (Start Date)
    Stop Date (e.g. 31 May 03)
    Descripción

    Stop Date

    Tipo de datos

    date

    Alias
    UMLS CUI [1,1]
    C0013227 (Pharmaceutical Preparations)
    SNOMED
    763158003
    LOINC
    LP100609-9
    UMLS CUI [1,2]
    C0806020 (End date)
    SNOMED
    454551000124105
    LOINC
    MTHU008302
    Ongoing Medication? (e.g. N)
    Descripción

    Ongoing Medication

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C2826666 (Concomitant Medication Ongoing)

    Similar models

    Concomitant Medications Open-Label Extension Assessing Long-Term Safety Of Rosiglitazone In Subjects With Mild To Moderate Alzheimer's Disease NCT00381238

    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    Alias
    Item Group
    Concomitant Medications
    C2347852 (UMLS CUI-1)
    Concomitant Medication
    Item
    Were any concomitant medications taken by the subject prior to screening and/or during the study? 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
    C0013227 (UMLS CUI [1,1])
    C0869039 (UMLS CUI [1,2])
    Units
    Item
    Units* (eg. mg)
    text
    C0013227 (UMLS CUI [1,1])
    C1519795 (UMLS CUI [1,2])
    Frequency
    Item
    Frequency* (e.g. BID)
    text
    C3476109 (UMLS CUI [1])
    Route
    Item
    Route* (e.g. PO)
    text
    C0013153 (UMLS CUI [1])
    Reason for Medication
    Item
    Reason for Medication (e.g. Headache)
    text
    C0013227 (UMLS CUI [1,1])
    C0392360 (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])
    Stop Date
    Item
    Stop Date (e.g. 31 May 03)
    date
    C0013227 (UMLS CUI [1,1])
    C0806020 (UMLS CUI [1,2])
    Ongoing Medication
    Item
    Ongoing Medication? (e.g. N)
    boolean
    C2826666 (UMLS CUI [1])

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