ID

29527

Descripción

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: Investigational Product Compliance

Palabras clave

Versiones (2)
  1. 4/3/18 4/3/18 -
  2. 5/4/18 5/4/18 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

5 de abril de 2018

DOI

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Licencia

Creative Commons BY-NC 3.0
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GSK Efficacy and safety of Fluticasone on the Annual Rate of Exacerbations in Subjects with Chronic Obstructive Pulmonary Disease (COPD) NCT01009463

Inglés

Investigational Product Compliance

1 formularios  
Investigational Product Compliance
Descripción

Investigational Product Compliance

Alias
UMLS CUI-1
C0304229
UMLS CUI-2
C1321605
Visit Investigational Product Dispensed
Descripción

Visit Investigational Product Dispensed

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0947323
UMLS CUI [1,3]
C0545082
Date lnvestigational Product Dispensed
Descripción

Date lnvestigational Product Dispensed

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0947323
UMLS CUI [1,3]
C0011008
Dose Counter Start
Descripción

Dose Counter Start

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0678766
UMLS CUI [1,2]
C0808070
Visit Investigational Product Returned
Descripción

Visit Investigational Product Returned

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0332156
UMLS CUI [1,3]
C0545082
Date lnvestigational Product Returned
Descripción

Date lnvestigational Product Returned

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0332156
UMLS CUI [1,3]
C0011008
Dose Counter Stop
Descripción

Dose Counter Stop

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0678766
UMLS CUI [1,2]
C0806020
lnvestigational product container number
Descripción

lnvestigational product container number

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0180098
UMLS CUI [1,3]
C0600091
Volver a la parte superior de la página

Similar models

Investigational Product Compliance

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Investigational Product Compliance
C0304229 (UMLS CUI-1)
C1321605 (UMLS CUI-2)
Visit Investigational Product Dispensed
Item
Visit Investigational Product Dispensed
text
C0304229 (UMLS CUI [1,1])
C0947323 (UMLS CUI [1,2])
C0545082 (UMLS CUI [1,3])
Date lnvestigational Product Dispensed
Item
Date lnvestigational Product Dispensed
date
C0304229 (UMLS CUI [1,1])
C0947323 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Dose Counter Start
Item
Dose Counter Start
text
C0678766 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Visit Investigational Product Returned
Item
Visit Investigational Product Returned
text
C0304229 (UMLS CUI [1,1])
C0332156 (UMLS CUI [1,2])
C0545082 (UMLS CUI [1,3])
Date lnvestigational Product Returned
Item
Date lnvestigational Product Returned
date
C0304229 (UMLS CUI [1,1])
C0332156 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Dose Counter Stop
Item
Dose Counter Stop
text
C0678766 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
lnvestigational product container number
Item
lnvestigational product container number
text
C0304229 (UMLS CUI [1,1])
C0180098 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,3])
Volver a la parte superior de la página 

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