ID

32545

Descripción

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

Palabras clave

Versiones (2)
  1. 6/11/18 6/11/18 -
  2. 6/12/18 6/12/18 -
Titular de derechos de autor

GSK group of companies

Subido en

6 de noviembre de 2018

DOI

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Licencia

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

Inglés

Run-In Failure Report

1 formularios  
  1. StudyEvent: ODM
    1. Run-In Failure Report
Run-In Failure
Descripción

Run-In Failure

Was this subject a run-in failure?
Descripción

Was this subject a run-in failure?

Tipo de datos

boolean

If YES, complete run-in reason
Descripción

If YES, complete run-in reason

Tipo de datos

text

If INVESTIGATOR DISCRETION, specify
Descripción

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

Tipo de datos

text

If WITHDREW CONSENT, specify
Descripción

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

Tipo de datos

text

Run-In Failure Date
Descripción

Run-In Failure Date

Tipo de datos

date

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Similar models

Run-In Failure Report

1 formularios
  1. StudyEvent: ODM
    1. Run-In Failure Report
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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
Volver a la parte superior de la página 

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