ID
29168
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: Serious Adverse Event
Nyckelord
Versioner (2)
- 2018-03-04 2018-03-04 -
- 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
Serious Adverse Event
- StudyEvent: ODM
Beskrivning
Intensity Changes
Alias
- UMLS CUI-1
- C1710066
- UMLS CUI-2
- C0518690
- UMLS CUI-3
- C1519255
Beskrivning
Serious Adverse Event
Datatyp
text
Alias
- UMLS CUI [1]
- C1519255
Beskrivning
Start Date of event segment
Datatyp
date
Alias
- UMLS CUI [1]
- C2697888
Beskrivning
Start Time of event segment
Datatyp
time
Alias
- UMLS CUI [1]
- C2697889
Beskrivning
Intensity of event segment
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0518690
Beskrivning
Grade of event segment
Datatyp
integer
Alias
- UMLS CUI [1]
- C2985911
Beskrivning
Grade or Intensity of event segment
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0518690
- UMLS CUI [2]
- C2985911
Beskrivning
Concomitant medication
Alias
- UMLS CUI-1
- C2347852
Beskrivning
Unit
Datatyp
text
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C1519795
Beskrivning
Frequency
Datatyp
text
Alias
- UMLS CUI [1]
- C3476109
Beskrivning
Route
Datatyp
text
Alias
- UMLS CUI [1]
- C0013153
Beskrivning
Drug Type
Datatyp
text
Alias
- UMLS CUI [1]
- C0457591
Beskrivning
Enter drug name, not description (Generic name preferred. If combination product, enter Trade name).
Datatyp
text
Alias
- UMLS CUI [1]
- C2360065
Beskrivning
eg. 500 mg
Datatyp
float
Alias
- UMLS CUI [1]
- C2348070
Beskrivning
Primary Indication
Datatyp
text
Alias
- UMLS CUI [1,1]
- C3146298
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [2]
- C0011900
Beskrivning
start date of medication
Datatyp
date
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0808070
Beskrivning
End Date of medication
Datatyp
date
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0806020
Beskrivning
If a medication was marked ‘Continuing’ at a previous visit, but has since had a dosage change or has been stopped, it must be recorded as a change below with the new start and end date.
Datatyp
boolean
Alias
- UMLS CUI [1]
- C2826666
Beskrivning
Relevant medical conditions/Risk factors
Alias
- UMLS CUI-1
- C0262926
- UMLS CUI-2
- C0035648
- UMLS CUI-3
- C1519255
Beskrivning
Specific Condition name
Datatyp
text
Alias
- UMLS CUI [1]
- C0012634
Beskrivning
Date of onset
Datatyp
date
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C0574845
Beskrivning
Continuing?
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C0549178
Beskrivning
date of last occurrence
Datatyp
date
Alias
- UMLS CUI [1,1]
- C2745955
- UMLS CUI [1,2]
- C0012634
- UMLS CUI [1,3]
- C0011008
Beskrivning
Relevant Diagnostic Results
Alias
- UMLS CUI-1
- C0430022
- UMLS CUI-2
- C0456984
Beskrivning
Normal High Range
Datatyp
text
Alias
- UMLS CUI [1]
- C0086715
Beskrivning
Relevant diagnostic results not noted above
Datatyp
text
Alias
- UMLS CUI [1]
- C0587081
Beskrivning
Test Name
Datatyp
text
Alias
- UMLS CUI [1]
- C0022885
Beskrivning
Test Date
Datatyp
date
Alias
- UMLS CUI [1]
- C2826247
Beskrivning
Test Result
Datatyp
text
Alias
- UMLS CUI [1]
- C0587081
Beskrivning
Test Units
Datatyp
text
Alias
- UMLS CUI [1,1]
- C1519795
- UMLS CUI [1,2]
- C0587081
Beskrivning
Normal Low Range
Datatyp
text
Alias
- UMLS CUI [1]
- C0086715
Beskrivning
Rechallenge
Alias
- UMLS CUI-1
- C2347900
- UMLS CUI-2
- C0304229
Beskrivning
Investigational product
Alias
- UMLS CUI-1
- C0304229
Beskrivning
Study Drug
Datatyp
text
Alias
- UMLS CUI [1]
- C0304229
Beskrivning
start date
Datatyp
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0808070
Beskrivning
stop date
Datatyp
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0806020
Beskrivning
Regimen
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C0237125
- UMLS CUI [1,2]
- C0304229
Similar models
Serious Adverse Event
- StudyEvent: ODM
C0304229 (UMLS CUI [1,2])
C0574845 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C1519255 (UMLS CUI [1,2])
C0085978 (UMLS CUI [1,2])
C1519255 (UMLS CUI [1,3])
C1519255 (UMLS CUI [1,2])
C1519255 (UMLS CUI [1,2])
C1519255 (UMLS CUI [1,2])
C0518690 (UMLS CUI-2)
C1519255 (UMLS CUI-3)
C0518690 (UMLS CUI [1,2])
C0518690 (UMLS CUI [1,2])
C2985911 (UMLS CUI [2])
C1519795 (UMLS CUI [1,2])
C2347852 (UMLS CUI [1,2])
C0011900 (UMLS CUI [2])
C0808070 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0035648 (UMLS CUI-2)
C1519255 (UMLS CUI-3)
C0574845 (UMLS CUI [1,2])
C0012634 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0456984 (UMLS CUI-2)
C0587081 (UMLS CUI [1,2])
C0034897 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,3])
C0808070 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,2])