ID

33181

Descrição

Study ID: 106837 Clinical Study ID: HZA106837 Study Title: A Long-Term, Randomized, Double-Blind, Parallel Group Study of Fluticasone Furoate/GW642444 Inhalation Powder Once-Daily and Fluticasone Furoate Inhalation Powder Once-Daily in Subjects with Asthma Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01086384 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: fluticasone furoate/vilanterol Trade Name: Relvar Study Indication: Asthma

Palavras-chave

Versões (2)
  1. 05/11/2018 05/11/2018 -
  2. 30/11/2018 30/11/2018 -
Titular dos direitos

GSK group of companies

Transferido a

30 de novembro de 2018

DOI

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Licença

Creative Commons BY-NC 3.0
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A Parallel Group Study of Fluticasone Furoate/Vilanterol in Subjects with Asthma - 106837

Inglês

Log Status Form

1 Formulários  
  1. StudyEvent: ODM
    1. Log Status Form
Log Status
Descrição

Log Status

Alias
UMLS CUI-1
C1708728
UMLS CUI-2
C0449438
Did the subject experience any non-serious adverse events during the study?
Descrição

Did the subject experience any non-serious adverse events during the study?

Tipo de dados

boolean

Alias
UMLS CUI [1]
C1518404
Were any concomitant medications taken by the subject during the study?
Descrição

Were any concomitant medications taken by the subject during the study?

Tipo de dados

boolean

Alias
UMLS CUI [1]
C2347852
Did the subject experience any exacerbation during the study?
Descrição

Did the subject experience any exacerbation during the study?

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0349790
Was a chest x-ray performed? (to confirm diagnosis of pneumonia)
Descrição

Was a chest x-ray performed? (to confirm diagnosis of pneumonia)

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0039985
UMLS CUI [2,1]
C0032285
UMLS CUI [2,2]
C0011900
Did any device(s) supplied to the subject malfunction during the course of the study?
Descrição

Did any device(s) supplied to the subject malfunction during the course of the study?

Tipo de dados

boolean

Alias
UMLS CUI [1]
C1881681
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Similar models

Log Status Form

1 Formulários
  1. StudyEvent: ODM
    1. Log Status Form
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
Log Status
C1708728 (UMLS CUI-1)
C0449438 (UMLS CUI-2)
Did the subject experience any non-serious adverse events during the study?
Item
Did the subject experience any non-serious adverse events during the study?
boolean
C1518404 (UMLS CUI [1])
Were any concomitant medications taken by the subject during the study?
Item
Were any concomitant medications taken by the subject during the study?
boolean
C2347852 (UMLS CUI [1])
Did the subject experience any exacerbation during the study?
Item
Did the subject experience any exacerbation during the study?
boolean
C0349790 (UMLS CUI [1])
Was a chest x-ray performed? (to confirm diagnosis of pneumonia)
Item
Was a chest x-ray performed? (to confirm diagnosis of pneumonia)
boolean
C0039985 (UMLS CUI [1])
C0032285 (UMLS CUI [2,1])
C0011900 (UMLS CUI [2,2])
Did any device(s) supplied to the subject malfunction during the course of the study?
Item
Did any device(s) supplied to the subject malfunction during the course of the study?
boolean
C1881681 (UMLS CUI [1])
Voltar ao início da página 

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