ID

29527

Beschrijving

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

Trefwoorden

  1. 04-03-18 04-03-18 -
  2. 05-04-18 05-04-18 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

5 april 2018

DOI

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Licentie

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

Investigational Product Compliance

Investigational Product Compliance
Beschrijving

Investigational Product Compliance

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

Visit Investigational Product Dispensed

Datatype

text

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

Date lnvestigational Product Dispensed

Datatype

date

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

Dose Counter Start

Datatype

text

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

Visit Investigational Product Returned

Datatype

text

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

Date lnvestigational Product Returned

Datatype

date

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

Dose Counter Stop

Datatype

text

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

lnvestigational product container number

Datatype

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0180098
UMLS CUI [1,3]
C0600091

Similar models

Investigational Product Compliance

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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])

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