0 Ratings
ID

29527

Description

Study ID: 102871 Clinical Study ID: HZC102871 Study Title:HZC102871: A 52-week efficacy and safety study to compare the effect of three dosage strengths of Fluticasone Furoate/GW642444 Inhalation Powder with GW642444 on the Annual Rate of Exacerbations in Subjects with Chronic Obstructive Pulmonary Disease (COPD) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01009463 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: fluticasone furoate Trade Name: Veramyst,Avamys,Allermist Study Indication: Pulmonary Disease, Chronic Obstructive Documentation part: Investigational Product Compliance

Keywords

Versions (2)
  1. 3/4/18 3/4/18 -
  2. 4/5/18 4/5/18 -
Copyright Holder

GlaxoSmithKline

Uploaded on

April 5, 2018

DOI

To request one please log in.

License

Creative Commons BY-NC 3.0
Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Back to model comments
Itemgroup comments for :

Item comments for :

  • Newest
  • Oldest
  • Popular
  • Newest
    • Newest
    • Oldest
    • Popular

    No comments

    In order to download data models you must be logged in. Please log in or register for free.

    GSK Efficacy and safety of Fluticasone on the Annual Rate of Exacerbations in Subjects with Chronic Obstructive Pulmonary Disease (COPD) NCT01009463

    English

    Investigational Product Compliance

    1 forms  
    Investigational Product Compliance
    Description

    Investigational Product Compliance

    Alias
    UMLS CUI-1
    C0304229
    UMLS CUI-2
    C1321605
    Visit Investigational Product Dispensed
    Description

    Visit Investigational Product Dispensed

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0304229
    UMLS CUI [1,2]
    C0947323
    UMLS CUI [1,3]
    C0545082
    Date lnvestigational Product Dispensed
    Description

    Date lnvestigational Product Dispensed

    Data type

    date

    Alias
    UMLS CUI [1,1]
    C0304229
    UMLS CUI [1,2]
    C0947323
    UMLS CUI [1,3]
    C0011008
    Dose Counter Start
    Description

    Dose Counter Start

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0678766
    UMLS CUI [1,2]
    C0808070
    Visit Investigational Product Returned
    Description

    Visit Investigational Product Returned

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0304229
    UMLS CUI [1,2]
    C0332156
    UMLS CUI [1,3]
    C0545082
    Date lnvestigational Product Returned
    Description

    Date lnvestigational Product Returned

    Data type

    date

    Alias
    UMLS CUI [1,1]
    C0304229
    UMLS CUI [1,2]
    C0332156
    UMLS CUI [1,3]
    C0011008
    Dose Counter Stop
    Description

    Dose Counter Stop

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0678766
    UMLS CUI [1,2]
    C0806020
    lnvestigational product container number
    Description

    lnvestigational product container number

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0304229
    UMLS CUI [1,2]
    C0180098
    UMLS CUI [1,3]
    C0600091
    Back to the top of the page

    Similar models

    Investigational Product Compliance

    1 forms
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    Investigational Product Compliance
    C0304229 (UMLS CUI-1)
    C1321605 (UMLS CUI-2)
    Visit Investigational Product Dispensed
    Item
    Visit Investigational Product Dispensed
    text
    C0304229 (UMLS CUI [1,1])
    C0947323 (UMLS CUI [1,2])
    C0545082 (UMLS CUI [1,3])
    Date lnvestigational Product Dispensed
    Item
    Date lnvestigational Product Dispensed
    date
    C0304229 (UMLS CUI [1,1])
    C0947323 (UMLS CUI [1,2])
    C0011008 (UMLS CUI [1,3])
    Dose Counter Start
    Item
    Dose Counter Start
    text
    C0678766 (UMLS CUI [1,1])
    C0808070 (UMLS CUI [1,2])
    Visit Investigational Product Returned
    Item
    Visit Investigational Product Returned
    text
    C0304229 (UMLS CUI [1,1])
    C0332156 (UMLS CUI [1,2])
    C0545082 (UMLS CUI [1,3])
    Date lnvestigational Product Returned
    Item
    Date lnvestigational Product Returned
    date
    C0304229 (UMLS CUI [1,1])
    C0332156 (UMLS CUI [1,2])
    C0011008 (UMLS CUI [1,3])
    Dose Counter Stop
    Item
    Dose Counter Stop
    text
    C0678766 (UMLS CUI [1,1])
    C0806020 (UMLS CUI [1,2])
    lnvestigational product container number
    Item
    lnvestigational product container number
    text
    C0304229 (UMLS CUI [1,1])
    C0180098 (UMLS CUI [1,2])
    C0600091 (UMLS CUI [1,3])
    Back to the top of the page 

    Help

    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