ID

29525

Descrição

Study ID: 102871 Clinical Study ID: HZC102871 Study Title:HZC102871: A 52-week efficacy and safety study to compare the effect of three dosage strengths of Fluticasone Furoate/GW642444 Inhalation Powder with GW642444 on the Annual Rate of Exacerbations in Subjects with Chronic Obstructive Pulmonary Disease (COPD) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01009463 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: fluticasone furoate Trade Name: Veramyst,Avamys,Allermist Study Indication: Pulmonary Disease, Chronic Obstructive Documentation part: LOG Status

Palavras-chave

Versões (2)
  1. 04/03/2018 04/03/2018 -
  2. 05/04/2018 05/04/2018 -
Titular dos direitos

GlaxoSmithKline

Transferido a

5 de abril de 2018

DOI

Para um pedido faça login.

Licença

Creative Commons BY-NC 3.0
Comentários do modelo :

Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.

Voltar para os comentários do modelo
Comentários do grupo de itens para :

Comentários do item para :

Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.

GSK Efficacy and safety of Fluticasone on the Annual Rate of Exacerbations in Subjects with Chronic Obstructive Pulmonary Disease (COPD) NCT01009463

Inglês

LOG Status

1 Formulários  
  1. StudyEvent: ODM
    1. LOG Status
LOG Status
Descrição

LOG Status

Alias
UMLS CUI-1
C1708728
UMLS CUI-2
C0449438
Were any concomitant medications taken by the subject during the study?
Descrição

Concomitant medications

Tipo de dados

boolean

Alias
UMLS CUI [1]
C2347852
Did the subject experience any non-serious adverse events during the study?
Descrição

non-serious adverse event

Tipo de dados

boolean

Alias
UMLS CUI [1]
C1518404
Did the subject experience any COPD exacerbations?
Descrição

COPD exacerbations

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0740304
Has subject been diagnosed with pneumonia?
Descrição

pneumonia

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0032285
Did the subject have a fracture during the course of the study?
Descrição

fracture

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0016658
Did any Novel Dry Powder Inhaler device(s) supplied to the subject malfunction during the course of the study?
Descrição

device malfunction

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0025080
Voltar ao início da página

Similar models

LOG Status

1 Formulários
  1. StudyEvent: ODM
    1. LOG Status
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
LOG Status
C1708728 (UMLS CUI-1)
C0449438 (UMLS CUI-2)
Concomitant medications
Item
Were any concomitant medications taken by the subject during the study?
boolean
C2347852 (UMLS CUI [1])
non-serious adverse event
Item
Did the subject experience any non-serious adverse events during the study?
boolean
C1518404 (UMLS CUI [1])
COPD exacerbations
Item
Did the subject experience any COPD exacerbations?
boolean
C0740304 (UMLS CUI [1])
pneumonia
Item
Has subject been diagnosed with pneumonia?
boolean
C0032285 (UMLS CUI [1])
fracture
Item
Did the subject have a fracture during the course of the study?
boolean
C0016658 (UMLS CUI [1])
device malfunction
Item
Did any Novel Dry Powder Inhaler device(s) supplied to the subject malfunction during the course of the study?
boolean
C0025080 (UMLS CUI [1])
Voltar ao início da página 

Contacto

Use este formulário para feedback, perguntas e sugestões de aperfeiçoamento.

Campos marcados com * são obrigatórios.

Ajuda

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial