ID

33127

Beschrijving

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

Trefwoorden

Versies (2)
  1. 02-11-18 02-11-18 -
  2. 28-11-18 28-11-18 -
Houder van rechten

GSK group of companies

Geüploaded op

28 november 2018

DOI

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Licentie

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

Engels

Exacerbation History

1 Formulieren  
  1. StudyEvent: ODM
    1. Exacerbation History
History of Asthma Exacerbations
Beschrijving

History of Asthma Exacerbations

Alias
UMLS CUI-1
C0349790
UMLS CUI-2
C0262926
Record number of asthma exacerbations in the 12 months prior to Visit 1
Beschrijving

Record number of asthma exacerbations in the 12 months prior to Visit 1

Datatype

integer

Alias
UMLS CUI [1,1]
C0349790
UMLS CUI [1,2]
C0237753
UMLS CUI [1,3]
C0545082
UMLS CUI [1,4]
C0332152
1. Number of exacerbations in the last 12 months that were managed without oral/systemic corticosteroids (not involving hospitalisation)
Beschrijving

If none, enter 0 (zero)

Datatype

integer

Alias
UMLS CUI [1,1]
C0349790
UMLS CUI [1,2]
C0237753
UMLS CUI [2,1]
C2825233
UMLS CUI [2,2]
C1273870
UMLS CUI [3]
C0019993
2. Number of exacerbations in the last 12 months that required oral/systemic corticosteroids (not involving hospitalisation)
Beschrijving

If none, enter 0 (zero)

Datatype

integer

Alias
UMLS CUI [1,1]
C0349790
UMLS CUI [1,2]
C0237753
UMLS CUI [2,1]
C2825233
UMLS CUI [2,2]
C1273870
UMLS CUI [3]
C0019993
3. Number of exacerbations in the last 12 months that required hospitalisation (in-patient or Emergency Department)
Beschrijving

If none, enter 0 (zero)

Datatype

integer

Alias
UMLS CUI [1,1]
C0349790
UMLS CUI [1,2]
C0237753
UMLS CUI [2]
C0019993
UMLS CUI [3]
C3840745
Terug naar het begin van de pagina

Similar models

Exacerbation History

1 Formulieren
  1. StudyEvent: ODM
    1. Exacerbation History
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
History of Asthma Exacerbations
C0349790 (UMLS CUI-1)
C0262926 (UMLS CUI-2)
Record number of asthma exacerbations in the 12 months prior to Visit 1
Item
Record number of asthma exacerbations in the 12 months prior to Visit 1
integer
C0349790 (UMLS CUI [1,1])
C0237753 (UMLS CUI [1,2])
C0545082 (UMLS CUI [1,3])
C0332152 (UMLS CUI [1,4])
1. Number of exacerbations in the last 12 months that were managed without oral/systemic corticosteroids (not involving hospitalisation)
Item
1. Number of exacerbations in the last 12 months that were managed without oral/systemic corticosteroids (not involving hospitalisation)
integer
C0349790 (UMLS CUI [1,1])
C0237753 (UMLS CUI [1,2])
C2825233 (UMLS CUI [2,1])
C1273870 (UMLS CUI [2,2])
C0019993 (UMLS CUI [3])
2. Number of exacerbations in the last 12 months that required oral/systemic corticosteroids (not involving hospitalisation)
Item
2. Number of exacerbations in the last 12 months that required oral/systemic corticosteroids (not involving hospitalisation)
integer
C0349790 (UMLS CUI [1,1])
C0237753 (UMLS CUI [1,2])
C2825233 (UMLS CUI [2,1])
C1273870 (UMLS CUI [2,2])
C0019993 (UMLS CUI [3])
3. Number of exacerbations in the last 12 months that required hospitalisation (in-patient or Emergency Department)
Item
3. Number of exacerbations in the last 12 months that required hospitalisation (in-patient or Emergency Department)
integer
C0349790 (UMLS CUI [1,1])
C0237753 (UMLS CUI [1,2])
C0019993 (UMLS CUI [2])
C3840745 (UMLS CUI [3])
Terug naar het begin van de pagina 

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