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ID

24603

Beschrijving

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

Trefwoorden

Versies (2)
  1. 05-08-17 05-08-17 -
  2. 08-08-17 08-08-17 -
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8 augustus 2017

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Creative Commons BY-NC 3.0
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    follow-up salmeterol/fluticasone propionate combination compared to salmeterol on COPD 100470

    Engels

    follow-up salmeterol/fluticasone propionate combination compared to salmeterol on COPD 100470

    1 Formulieren  
    Administrative Data
    Beschrijving

    Administrative Data

    Alias
    UMLS CUI-1
    C1320722
    Subject Identifier
    Beschrijving

    subject identifier

    Datatype

    integer

    Alias
    UMLS CUI [1]
    C2348585
    Visit Date
    Beschrijving

    date of visit

    Datatype

    date

    Alias
    UMLS CUI [1]
    C1320303
    OROPHARYNGEAL CANDIDIASIS EXAMINATION
    Beschrijving

    OROPHARYNGEAL CANDIDIASIS EXAMINATION

    Alias
    UMLS CUI-1
    C0006849
    UMLS CUI-2
    C0582103
    Does the subject have clinical evidence of oropharyngeal candidiasis?
    Beschrijving

    clinical evidence of oropharyngeal candidiasis

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C0006849
    UMLS CUI [1,2]
    C3887511
    Was a swab taken?
    Beschrijving

    Swab need only be taken if there is clinical evidence of oropharyngeal candidiasis

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C0006849
    UMLS CUI [1,2]
    C0563454
    if a swab was taken, result of the swab?
    Beschrijving

    oropharyngeal candidiasis test result

    Datatype

    integer

    Alias
    UMLS CUI [1,1]
    C0006849
    UMLS CUI [1,2]
    C0563454
    UMLS CUI [1,3]
    C1274040
    VITAL SIGNS
    Beschrijving

    VITAL SIGNS

    Alias
    UMLS CUI-1
    C0518766
    Blood pressure
    Beschrijving

    Position: sitting

    Datatype

    integer

    Maateenheden
    • mmHg
    Alias
    UMLS CUI [1]
    C0005823
    mmHg
    Heart rate
    Beschrijving

    heart rate

    Datatype

    integer

    Maateenheden
    • bpm
    Alias
    UMLS CUI [1]
    C0018810
    bpm
    CENTRAL LABORATORY - BLOOD
    Beschrijving

    CENTRAL LABORATORY - BLOOD

    Alias
    UMLS CUI-1
    C0018941
    Date sample taken
    Beschrijving

    blood sample taken

    Datatype

    date

    Alias
    UMLS CUI [1]
    C1277698
    Terug naar het begin van de pagina

    Similar models

    follow-up salmeterol/fluticasone propionate combination compared to salmeterol on COPD 100470

    1 Formulieren
    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    Administrative Data
    C1320722 (UMLS CUI-1)
    subject identifier
    Item
    Subject Identifier
    integer
    C2348585 (UMLS CUI [1])
    date of visit
    Item
    Visit Date
    date
    C1320303 (UMLS CUI [1])
    Item Group
    OROPHARYNGEAL CANDIDIASIS EXAMINATION
    C0006849 (UMLS CUI-1)
    C0582103 (UMLS CUI-2)
    Item
    Does the subject have clinical evidence of oropharyngeal candidiasis?
    text
    C0006849 (UMLS CUI [1,1])
    C3887511 (UMLS CUI [1,2])
    clinical evidence of oropharyngeal candidiasis
    Code List
    Does the subject have clinical evidence of oropharyngeal candidiasis?
    CL Item
    Yes (Y)
    CL Item
    No (N)
    Item
    Was a swab taken?
    text
    C0006849 (UMLS CUI [1,1])
    C0563454 (UMLS CUI [1,2])
    taking of a swab
    Code List
    Was a swab taken?
    CL Item
    Yes (Y)
    CL Item
    No (N)
    Item
    if a swab was taken, result of the swab?
    integer
    C0006849 (UMLS CUI [1,1])
    C0563454 (UMLS CUI [1,2])
    C1274040 (UMLS CUI [1,3])
    oropharyngeal candidiasis test result
    Code List
    if a swab was taken, result of the swab?
    CL Item
    Negative (1)
    CL Item
    Positive (2)
    CL Item
    Not available (4)
    Item Group
    VITAL SIGNS
    C0518766 (UMLS CUI-1)
    blood pressure
    Item
    Blood pressure
    integer
    C0005823 (UMLS CUI [1])
    heart rate
    Item
    Heart rate
    integer
    C0018810 (UMLS CUI [1])
    Item Group
    CENTRAL LABORATORY - BLOOD
    C0018941 (UMLS CUI-1)
    blood sample taken
    Item
    Date sample taken
    date
    C1277698 (UMLS CUI [1])
    Terug naar het begin van de pagina 

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