ID

33369

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

  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

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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

Pregnancy Information

  1. StudyEvent: ODM
    1. Pregnancy Information
Pregnancy Information
Descripción

Pregnancy Information

Alias
UMLS CUI-1
C0032961
UMLS CUI-2
C1533716
Did the subject become pregnant during the study?
Descripción

Did the subject become pregnant during the study?

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0008976
if YES, complete the paper Pregnancy Notification form
Descripción

if YES, complete the paper Pregnancy Notification form

Tipo de datos

text

Alias
UMLS CUI [1]
C0032961

Similar models

Pregnancy Information

  1. StudyEvent: ODM
    1. Pregnancy Information
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Pregnancy Information
C0032961 (UMLS CUI-1)
C1533716 (UMLS CUI-2)
Did the subject become pregnant during the study?
Item
Did the subject become pregnant during the study?
boolean
C0032961 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
if YES, complete the paper Pregnancy Notification form
Item
if YES, complete the paper Pregnancy Notification form
text
C0032961 (UMLS CUI [1])

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