ID

33297

Beskrivning

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

Nyckelord

Versioner (2)
  1. 2018-11-05 2018-11-05 -
  2. 2018-12-04 2018-12-04 -
Rättsinnehavare

GSK group of companies

Uppladdad den

4 december 2018

DOI

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Licens

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

Engelsk

Chest X-Ray Data

1 Formulär  
  1. StudyEvent: ODM
    1. Chest X-Ray Data
Chest X-Ray
Beskrivning

Chest X-Ray

Alias
UMLS CUI-1
C0039985
Date of x-ray
Beskrivning

A confirmatory chest x-ray should be considered for adverse events of pneumonia. Confirmed diagnosis of pneumonia must be recorded as an Adverse Event. A chest x-ray should be obtained within 48 hours of suspected pneumonia.

Datatyp

date

Alias
UMLS CUI [1,1]
C0039985
UMLS CUI [1,2]
C0011008
Were findings consistent with a diagnosis of pneumonia?
Beskrivning

Were findings consistent with a diagnosis of pneumonia?

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0032285
UMLS CUI [1,2]
C0243095
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Similar models

Chest X-Ray Data

1 Formulär
  1. StudyEvent: ODM
    1. Chest X-Ray Data
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Chest X-Ray
C0039985 (UMLS CUI-1)
Date of x-ray
Item
Date of x-ray
date
C0039985 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Were findings consistent with a diagnosis of pneumonia?
Item
Were findings consistent with a diagnosis of pneumonia?
boolean
C0032285 (UMLS CUI [1,1])
C0243095 (UMLS CUI [1,2])
Tillbaka till toppen 

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