ID

33361

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 diciembre de 2018

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY-NC 3.0
Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Volver a los comentarios del modelo
Comentarios de grupo de elementos para :

Comentarios del elemento para :

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

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

Alias
UMLS CUI-1
C1710476
Was this subject a run-in failure?
Descripción

Was this subject a run-in failure?

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1710476
UMLS CUI [1,2]
C0681850
If YES, complete run-in reason
Descripción

If YES, complete run-in reason

Tipo de datos

text

Alias
UMLS CUI [1,1]
C1710476
UMLS CUI [1,2]
C0392360
If INVESTIGATOR DISCRETION, specify
Descripción

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

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0008961
UMLS CUI [1,2]
C0022423
UMLS CUI [1,3]
C2348235
If WITHDREW CONSENT, specify
Descripción

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

Tipo de datos

text

Alias
UMLS CUI [1,1]
C1707492
UMLS CUI [1,2]
C2348235
Run-In Failure Date
Descripción

Run-In Failure Date

Tipo de datos

date

Alias
UMLS CUI [1,1]
C1710476
UMLS CUI [1,2]
C0011008
Volver a la parte superior de la página

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
C1710476 (UMLS CUI-1)
Was this subject a run-in failure?
Item
Was this subject a run-in failure?
boolean
C1710476 (UMLS CUI [1,1])
C0681850 (UMLS CUI [1,2])
Item
If YES, complete run-in reason
text
C1710476 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
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
C0008961 (UMLS CUI [1,1])
C0022423 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,3])
If WITHDREW CONSENT, specify
Item
If WITHDREW CONSENT, specify
text
C1707492 (UMLS CUI [1,1])
C2348235 (UMLS CUI [1,2])
Run-In Failure Date
Item
Run-In Failure Date
date
C1710476 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Volver a la parte superior de la página 

Contacto

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Ayuda

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