ID

29171

Beskrivning

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

Nyckelord

Versioner (2)
  1. 2018-03-04 2018-03-04 -
  2. 2018-04-05 2018-04-05 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

4 mars 2018

DOI

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Licens

Creative Commons BY-NC 3.0
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Efficacy and safety of Fluticasone on the Annual Rate of Exacerbations in Subjects with Chronic Obstructive Pulmonary Disease (COPD) GSK102871

Engelsk

Investigational Product Compliance

1 Formulär  
Investigational Product Compliance
Beskrivning

Investigational Product Compliance

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

Visit Investigational Product Dispensed

Datatyp

text

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

Date lnvestigational Product Dispensed

Datatyp

date

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

Dose Counter Start

Datatyp

text

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

Visit Investigational Product Returned

Datatyp

text

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

Date lnvestigational Product Returned

Datatyp

date

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

Dose Counter Stop

Datatyp

text

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

lnvestigational product container number

Datatyp

text

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

Similar models

Investigational Product Compliance

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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])
Tillbaka till toppen 

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