ID

32545

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. 06-11-18 06-11-18 -
  2. 06-12-18 06-12-18 -
Houder van rechten

GSK group of companies

Geüploaded op

6 november 2018

DOI

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Licentie

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

Engels

Run-In Failure Report

1 Formulieren  
  1. StudyEvent: ODM
    1. Run-In Failure Report
Run-In Failure
Beschrijving

Run-In Failure

Was this subject a run-in failure?
Beschrijving

Was this subject a run-in failure?

Datatype

boolean

If YES, complete run-in reason
Beschrijving

If YES, complete run-in reason

Datatype

text

If INVESTIGATOR DISCRETION, specify
Beschrijving

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

Datatype

text

If WITHDREW CONSENT, specify
Beschrijving

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

Datatype

text

Run-In Failure Date
Beschrijving

Run-In Failure Date

Datatype

date

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Similar models

Run-In Failure Report

1 Formulieren
  1. StudyEvent: ODM
    1. Run-In Failure Report
Name
Type
Description | Question | Decode (Coded Value)
Datatype
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
Terug naar het begin van de pagina 

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