ID

33122

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. 10/30/18 10/30/18 -
  2. 11/28/18 11/28/18 -
Houder van rechten

GSK group of companies

Geüploaded op

November 28, 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 :

  • Nieuwste
  • Oudste
  • Populair
  • Nieuwste
    • Nieuwste
    • Oudste
    • Populair

Geen commentaren

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

Screen Failure Form

1 Formulieren  
  1. StudyEvent: ODM
    1. Screen Failure Form
Screen Failure Data
Beschrijving

Screen Failure Data

Alias
UMLS CUI-1
C1710476
Was this subject a screen failure?
Beschrijving

Was this subject a screen failure?

Datatype

boolean

Alias
UMLS CUI [1,1]
C1710476
UMLS CUI [1,2]
C0681850
Screen Failure Date
Beschrijving

Screen Failure Date

Datatype

date

Alias
UMLS CUI [1,1]
C1710476
UMLS CUI [1,2]
C0011008
If YES, please select reason
Beschrijving

If YES, please select reason

Datatype

integer

Alias
UMLS CUI [1,1]
C1710476
UMLS CUI [1,2]
C0392360
Terug naar het begin van de pagina

Similar models

Screen Failure Form

1 Formulieren
  1. StudyEvent: ODM
    1. Screen Failure Form
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Screen Failure Data
C1710476 (UMLS CUI-1)
Was this subject a screen failure?
Item
Was this subject a screen failure?
boolean
C1710476 (UMLS CUI [1,1])
C0681850 (UMLS CUI [1,2])
Screen Failure Date
Item
Screen Failure Date
date
C1710476 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
If YES, please select reason
integer
C1710476 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
If YES, please select reason
Code List
If YES, please select reason
CL Item
Did not meet inclusion/exclusion criteria (1)
CL Item
Adverse Event (unspecified) (2)
CL Item
Study closed/terminated  (3)
CL Item
Investigator discretion, specify_____ (4)
CL Item
withdrew consent, specify______ (5)
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