ID

40696

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

Keywords

Versions (3)
  1. 11/2/18 11/2/18 -
  2. 11/29/18 11/29/18 -
  3. 4/30/20 4/30/20 - Sarah Riepenhausen
Copyright Holder

GSK group of companies

Uploaded on

April 30, 2020

DOI

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License

Creative Commons BY-NC 4.0
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A Parallel Group Study of Fluticasone Furoate/Vilanterol in Subjects with Asthma - 106837

English

SAE Status

1 forms  
  1. StudyEvent: ODM
    1. SAE Status
SAE Status
Description

SAE Status

Alias
UMLS CUI-1
C1519255
UMLS CUI-2
C0449438
Did the subject experience a serious adverse event during the study?
Description

If YES, record details in Serious Adverse Events Form.

Data type

boolean

Alias
UMLS CUI [1,1]
C1519255
UMLS CUI [1,2]
C0596545
If YES, record details in Serious Adverse Events Form
Description

If YES, record details in Serious Adverse Events Form

Data type

text

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Similar models

SAE Status

1 forms
  1. StudyEvent: ODM
    1. SAE Status
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
SAE Status
C1519255 (UMLS CUI-1)
C0449438 (UMLS CUI-2)
Did the subject experience a serious adverse event during the study?
Item
Did the subject experience a serious adverse event during the study?
boolean
C1519255 (UMLS CUI [1,1])
C0596545 (UMLS CUI [1,2])
If YES, record details in Serious Adverse Events Form
Item
If YES, record details in Serious Adverse Events Form
text
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