ID
29168
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: Serious Adverse Event
Palabras clave
Versiones (2)
- 4/3/18 4/3/18 -
- 5/4/18 5/4/18 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
4 de marzo de 2018
DOI
Para solicitar uno, por favor iniciar sesión.
Licencia
Creative Commons BY-NC 3.0
Comentarios del modelo :
Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.
Comentarios de grupo de elementos para :
Comentarios del elemento para :
Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.
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
Descripción
Intensity Changes
Alias
- UMLS CUI-1
- C1710066
- UMLS CUI-2
- C0518690
- UMLS CUI-3
- C1519255
Descripción
Serious Adverse Event
Tipo de datos
text
Alias
- UMLS CUI [1]
- C1519255
Descripción
Start Date of event segment
Tipo de datos
date
Alias
- UMLS CUI [1]
- C2697888
Descripción
Start Time of event segment
Tipo de datos
time
Alias
- UMLS CUI [1]
- C2697889
Descripción
Intensity of event segment
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0518690
Descripción
Grade of event segment
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C2985911
Descripción
Grade or Intensity of event segment
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0518690
- UMLS CUI [2]
- C2985911
Descripción
Concomitant medication
Alias
- UMLS CUI-1
- C2347852
Descripción
Unit
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C1519795
Descripción
Frequency
Tipo de datos
text
Alias
- UMLS CUI [1]
- C3476109
Descripción
Route
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0013153
Descripción
Drug Type
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0457591
Descripción
Enter drug name, not description (Generic name preferred. If combination product, enter Trade name).
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2360065
Descripción
eg. 500 mg
Tipo de datos
float
Alias
- UMLS CUI [1]
- C2348070
Descripción
Primary Indication
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C3146298
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [2]
- C0011900
Descripción
start date of medication
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0808070
Descripción
End Date of medication
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0806020
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C2826666
Descripción
Relevant medical conditions/Risk factors
Alias
- UMLS CUI-1
- C0262926
- UMLS CUI-2
- C0035648
- UMLS CUI-3
- C1519255
Descripción
Specific Condition name
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0012634
Descripción
Date of onset
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C0574845
Descripción
Continuing?
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C0549178
Descripción
date of last occurrence
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C2745955
- UMLS CUI [1,2]
- C0012634
- UMLS CUI [1,3]
- C0011008
Descripción
Relevant Diagnostic Results
Alias
- UMLS CUI-1
- C0430022
- UMLS CUI-2
- C0456984
Descripción
Normal High Range
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0086715
Descripción
Relevant diagnostic results not noted above
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0587081
Descripción
Test Name
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0022885
Descripción
Test Date
Tipo de datos
date
Alias
- UMLS CUI [1]
- C2826247
Descripción
Test Result
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0587081
Descripción
Test Units
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1519795
- UMLS CUI [1,2]
- C0587081
Descripción
Normal Low Range
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0086715
Descripción
Rechallenge
Alias
- UMLS CUI-1
- C2347900
- UMLS CUI-2
- C0304229
Descripción
event recur after investigational products were restarted
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0034897
- UMLS CUI [1,3]
- C0304229
Descripción
Investigational product
Alias
- UMLS CUI-1
- C0304229
Descripción
Study Drug
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0304229
Descripción
start date
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0808070
Descripción
stop date
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0806020
Descripción
Regimen
Tipo de datos
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])