ID

32492

Description

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

Mots-clés

Versions (2)
  1. 05/11/2018 05/11/2018 -
  2. 30/11/2018 30/11/2018 -
Détendeur de droits

GSK group of companies

Téléchargé le

5 novembre 2018

DOI

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Licence

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

Anglais

Log Status Form

1 Formulaires  
  1. StudyEvent: ODM
    1. Log Status Form
Log Status
Description

Log Status

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

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

Type de données

boolean

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

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

Type de données

boolean

Did the subject experience any exacerbation during the study?
Description

Did the subject experience any exacerbation during the study?

Type de données

boolean

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

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

Type de données

boolean

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

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

Type de données

boolean

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Similar models

Log Status Form

1 Formulaires
  1. StudyEvent: ODM
    1. Log Status Form
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Log Status
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
Were any concomitant medications taken by the subject during the study?
Item
Were any concomitant medications taken by the subject during the study?
boolean
Did the subject experience any exacerbation during the study?
Item
Did the subject experience any exacerbation during the study?
boolean
Was a chest x-ray performed? (to confirm diagnosis of pneumonia)
Item
Was a chest x-ray performed? (to confirm diagnosis of pneumonia)
boolean
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
Retour au début de la page 

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