0 Ratings
ID

24755

Description

Study ID: 100470 Clinical Study ID: SCO100470 Study Title: A multicentre, randomised, double-blind, parallel group, 24 week study to compare the effect of salmeterol/fluticasone propionate combination product 50/250mcg, with salmeterol 50mcg both delivered twice daily via DISKUS®/ACCUHALER® inhaler on lung function and dyspnoea in subjects with Chronic Obstructive Pulmonary Disease (COPD). Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: N/A Sponsor:GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: fluticasone propionate/salmeterol Trade Name: Serevent Study Indication: Pulmonary Disease, Chronic Obstructive

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Versions (1)
  1. 8/16/17 8/16/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

August 16, 2017

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License

Creative Commons BY-NC 3.0
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    transition dyspnoea index salmeterol/fluticasone propionate combination compared to salmeterol on COPD 100470

    English

    transition dyspnoea index salmeterol/fluticasone propionate combination compared to salmeterol on COPD 100470

    1 forms  
    Administrative Data
    Description

    Administrative Data

    Alias
    UMLS CUI-1
    C1320722
    Subject Identifier
    Description

    subject identifier

    Data type

    integer

    Alias
    UMLS CUI [1]
    C2348585
    TRANSITION DYSPNOEA INDEX (TDI)
    Description

    TRANSITION DYSPNOEA INDEX (TDI)

    Alias
    UMLS CUI-1
    C3714807
    Date of assessment
    Description

    date of assessment

    Data type

    date

    Alias
    UMLS CUI [1]
    C2985720
    visit description
    Description

    visit description

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0545082
    UMLS CUI [1,2]
    C0678257
    TDI Score
    Description

    transition dyspnoea index

    Data type

    integer

    Alias
    UMLS CUI [1]
    C3714807
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    Similar models

    transition dyspnoea index salmeterol/fluticasone propionate combination compared to salmeterol on COPD 100470

    1 forms
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    Administrative Data
    C1320722 (UMLS CUI-1)
    subject identifier
    Item
    Subject Identifier
    integer
    C2348585 (UMLS CUI [1])
    Item Group
    TRANSITION DYSPNOEA INDEX (TDI)
    C3714807 (UMLS CUI-1)
    date of assessment
    Item
    Date of assessment
    date
    C2985720 (UMLS CUI [1])
    Item
    visit description
    text
    C0545082 (UMLS CUI [1,1])
    C0678257 (UMLS CUI [1,2])
    visit description
    Code List
    visit description
    CL Item
    Visit 3 (Visit 3)
    CL Item
    Visit 4 (Visit 4)
    CL Item
    Visit 5 (Visit 5)
    CL Item
    Visit 6 (Visit 6)
    CL Item
    Visit 7 (Visit 7)
    CL Item
    Visit 8 (Visit 8)
    CL Item
    Withdrawal (Withdrawal)
    transition dyspnoea index
    Item
    TDI Score
    integer
    C3714807 (UMLS CUI [1])
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