ID

33371

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

  1. 11/6/18 11/6/18 -
  2. 12/6/18 12/6/18 -
Copyright Holder

GSK group of companies

Uploaded on

December 6, 2018

DOI

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License

Creative Commons BY-NC 3.0

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A Parallel Group Study of Fluticasone Furoate/Vilanterol in Subjects with Asthma - 106837

Follow-Up Contact

  1. StudyEvent: ODM
    1. Follow-Up Contact
Follow-Up contact question
Description

Follow-Up contact question

Alias
UMLS CUI-1
C1522577
UMLS CUI-2
C1705415
Subject contacted for follow-up?
Description

Subject contacted for follow-up?

Data type

boolean

Alias
UMLS CUI [1,1]
C1522577
UMLS CUI [1,2]
C1705415
If YES, record date of contact
Description

If YES, record date of contact

Data type

date

Alias
UMLS CUI [1,1]
C1522577
UMLS CUI [1,2]
C1705415
UMLS CUI [1,3]
C0011008

Similar models

Follow-Up Contact

  1. StudyEvent: ODM
    1. Follow-Up Contact
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Follow-Up contact question
C1522577 (UMLS CUI-1)
C1705415 (UMLS CUI-2)
Subject contacted for follow-up?
Item
Subject contacted for follow-up?
boolean
C1522577 (UMLS CUI [1,1])
C1705415 (UMLS CUI [1,2])
If YES, record date of contact
Item
If YES, record date of contact
date
C1522577 (UMLS CUI [1,1])
C1705415 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])

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