0 Avaliações

ID

24750

Descrição

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

Palavras-chave

  1. 16/08/2017 16/08/2017 -
  2. 16/08/2017 16/08/2017 -
  3. 16/08/2017 16/08/2017 -
Transferido a

16 de agosto de 2017

DOI

Para um pedido faça login.

Licença

Creative Commons BY-NC 3.0

Comentários do modelo :

Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.

Comentários do grupo de itens para :

Comentários do item para :


    Sem comentários

    Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.

    daily record card salmeterol/fluticasone propionate combination compared to salmeterol on COPD 100470

    daily record card salmeterol/fluticasone propionate combination compared to salmeterol on COPD 100470

    Administrative Data
    Descrição

    Administrative Data

    Alias
    UMLS CUI-1
    C1320722 (Administrative documentation)
    SNOMED
    405624007
    time of documentation
    Descrição

    time of documentation

    Tipo de dados

    text

    Alias
    UMLS CUI [1,1]
    C0040223 (Time)
    SNOMED
    410670007
    LOINC
    LP73517-2
    UMLS CUI [1,2]
    C0920316 (Documentation)
    LOINC
    LA17600-0
    Subject Identifier
    Descrição

    subject identifier

    Tipo de dados

    integer

    Alias
    UMLS CUI [1]
    C2348585 (Clinical Trial Subject Unique Identifier)
    Doctor’s name
    Descrição

    doctor's name

    Tipo de dados

    text

    Alias
    UMLS CUI [1]
    C2361125 (Attending physician name)
    LOINC
    MTHU028124
    Hospital/Clinic address
    Descrição

    hospital address

    Tipo de dados

    text

    Alias
    UMLS CUI [1,1]
    C0019994 (Hospitals)
    UMLS CUI [1,2]
    C1442065 (Address)
    SNOMED
    397635003
    LOINC
    LP96251-1
    Hospital/Clinic telephone number
    Descrição

    hospital telephone number

    Tipo de dados

    integer

    Alias
    UMLS CUI [1]
    C2986429 (Healthcare Facility Telecom Address)
    Next Clinic Visit
    Descrição

    Next Clinic Visit

    Alias
    UMLS CUI-1
    C0008952 (Clinic Visits)
    Date of next clinic visit
    Descrição

    date of next clinic visit

    Tipo de dados

    date

    Alias
    UMLS CUI [1]
    C2735342 (Date next clinic visit)
    LOINC
    LP96939-1
    Time of next clinic visit
    Descrição

    time of next clinic visit

    Tipo de dados

    time

    Alias
    UMLS CUI [1,1]
    C0008952 (Clinic Visits)
    UMLS CUI [1,2]
    C0040223 (Time)
    SNOMED
    410670007
    LOINC
    LP73517-2

    Similar models

    daily record card salmeterol/fluticasone propionate combination compared to salmeterol on COPD 100470

    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de dados
    Alias
    Item Group
    Administrative Data
    C1320722 (UMLS CUI-1)
    Item
    time of documentation
    text
    C0040223 (UMLS CUI [1,1])
    C0920316 (UMLS CUI [1,2])
    Code List
    time of documentation
    CL Item
    run-in period (RUN-IN PERIOD)
    CL Item
    treatment period visit 2 (TREATMENT PERIOD Visit 2)
    CL Item
    treatment period visit 3 (TREATMENT PERIOD Visit 3)
    CL Item
    treatment period visit 4 (TREATMENT PERIOD Visit 4)
    CL Item
    treatment period visit 5 (TREATMENT PERIOD Visit 5)
    CL Item
    treatment period visit 6 (TREATMENT PERIOD Visit 6)
    CL Item
    treatment period visit 7 (TREATMENT PERIOD Visit 7)
    subject identifier
    Item
    Subject Identifier
    integer
    C2348585 (UMLS CUI [1])
    doctor's name
    Item
    Doctor’s name
    text
    C2361125 (UMLS CUI [1])
    hospital address
    Item
    Hospital/Clinic address
    text
    C0019994 (UMLS CUI [1,1])
    C1442065 (UMLS CUI [1,2])
    hospital telephone number
    Item
    Hospital/Clinic telephone number
    integer
    C2986429 (UMLS CUI [1])
    Item Group
    Next Clinic Visit
    C0008952 (UMLS CUI-1)
    date of next clinic visit
    Item
    Date of next clinic visit
    date
    C2735342 (UMLS CUI [1])
    time of next clinic visit
    Item
    Time of next clinic visit
    time
    C0008952 (UMLS CUI [1,1])
    C0040223 (UMLS CUI [1,2])

    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