ID

32492

Beschreibung

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

Stichworte

Versionen (2)
  1. 05.11.18 05.11.18 -
  2. 30.11.18 30.11.18 -
Rechteinhaber

GSK group of companies

Hochgeladen am

5. November 2018

DOI

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Lizenz

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

Englisch

Log Status Form

1 Formulare  
  1. StudyEvent: ODM
    1. Log Status Form
Log Status
Beschreibung

Log Status

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

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

Datentyp

boolean

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

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

Datentyp

boolean

Did the subject experience any exacerbation during the study?
Beschreibung

Did the subject experience any exacerbation during the study?

Datentyp

boolean

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

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

Datentyp

boolean

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

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

Datentyp

boolean

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Ähnliche Modelle

Log Status Form

1 Formulare
  1. StudyEvent: ODM
    1. Log Status Form
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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
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