ID

32492

Beschrijving

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

Trefwoorden

Versies (2)
  1. 05-11-18 05-11-18 -
  2. 30-11-18 30-11-18 -
Houder van rechten

GSK group of companies

Geüploaded op

5 november 2018

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY-NC 3.0
Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Terug naar het model Commentaren
Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

A Parallel Group Study of Fluticasone Furoate/Vilanterol in Subjects with Asthma - 106837

Engels

Log Status Form

1 Formulieren  
  1. StudyEvent: ODM
    1. Log Status Form
Log Status
Beschrijving

Log Status

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

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

Datatype

boolean

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

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

Datatype

boolean

Did the subject experience any exacerbation during the study?
Beschrijving

Did the subject experience any exacerbation during the study?

Datatype

boolean

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

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

Datatype

boolean

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

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

Datatype

boolean

Terug naar het begin van de pagina

Similar models

Log Status Form

1 Formulieren
  1. StudyEvent: ODM
    1. Log Status Form
Name
Type
Description | Question | Decode (Coded Value)
Datatype
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
Terug naar het begin van de pagina 

Contact

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Help

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