ID

32545

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. 06/11/2018 06/11/2018 -
  2. 06/12/2018 06/12/2018 -
Détendeur de droits

GSK group of companies

Téléchargé le

6 novembre 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0
Modèle Commentaires :

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

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Run-In Failure Report

1 Formulaires  
  1. StudyEvent: ODM
    1. Run-In Failure Report
Run-In Failure
Description

Run-In Failure

Was this subject a run-in failure?
Description

Was this subject a run-in failure?

Type de données

boolean

If YES, complete run-in reason
Description

If YES, complete run-in reason

Type de données

text

If INVESTIGATOR DISCRETION, specify
Description

Select this reason if none of the other primary reasons are appropriate

Type de données

text

If WITHDREW CONSENT, specify
Description

Select this reason if none of the other primary reasons are appropriate

Type de données

text

Run-In Failure Date
Description

Run-In Failure Date

Type de données

date

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Similar models

Run-In Failure Report

1 Formulaires
  1. StudyEvent: ODM
    1. Run-In Failure Report
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Run-In Failure
Was this subject a run-in failure?
Item
Was this subject a run-in failure?
boolean
Item
If YES, complete run-in reason
text
If YES, complete run-in reason
Code List
If YES, complete run-in reason
CL Item
Adverse event (record details on the Non-Serious Adverse Events or Serious Adverse Events forms as appropriate) (1)
CL Item
Protocol Deviation (2)
CL Item
Study closed/terminated (3)
CL Item
Lost to Follow-up (4)
CL Item
Investigator discretion (5)
CL Item
Withdrew consent (6)
CL Item
Did not meet continuation criteria (7)
If INVESTIGATOR DISCRETION, specify
Item
If INVESTIGATOR DISCRETION, specify
text
If WITHDREW CONSENT, specify
Item
If WITHDREW CONSENT, specify
text
Run-In Failure Date
Item
Run-In Failure Date
date
Retour au début de la page 

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