COPD excerbation salmeterol/fluticasone propionate combination compared to salmeterol on COPD 100470

COPD EXACERBATIONS
Description

COPD EXACERBATIONS

Alias
UMLS CUI-1
C0740304
Was there a COPD exacerbation?
Description

COPD exacerbation

Data type

text

Alias
UMLS CUI [1]
C0740304
If "yes" to COPD exacerbation, record following items.
Description

If "yes" to COPD exacerbation, record following items.

Alias
UMLS CUI-1
C0740304
Date of Onset
Description

date of onset of COPD exacerbation

Data type

date

Alias
UMLS CUI [1,1]
C0574845
UMLS CUI [1,2]
C0740304
Outcome
Description

outcome of COPD exacerbation

Data type

integer

Alias
UMLS CUI [1,1]
C0085565
UMLS CUI [1,2]
C0740304
Date of Resolution or Death
Description

date of resolution or death

Data type

date

Alias
UMLS CUI [1]
C2985858
UMLS CUI [2]
C1148348
Severity
Description

severity of COPD excerbation

Data type

integer

Alias
UMLS CUI [1,1]
C0439793
UMLS CUI [1,2]
C0740304
Was the subject withdrawn due to this exacerbation?
Description

Subjects who experience more than one moderate exacerbation requiring antibiotic and/or oral corticosteroid treatment during the treatment period and/or experience a severe exacerbation requiring hospitalisation during the course of the study must be withdrawn.

Data type

text

Alias
UMLS CUI [1,1]
C0422727
UMLS CUI [1,2]
C0740304

Similar models

COPD excerbation salmeterol/fluticasone propionate combination compared to salmeterol on COPD 100470

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
COPD EXACERBATIONS
C0740304 (UMLS CUI-1)
Item
Was there a COPD exacerbation?
text
C0740304 (UMLS CUI [1])
Code List
Was there a COPD exacerbation?
CL Item
Yes (Y)
CL Item
No (N)
Item Group
If "yes" to COPD exacerbation, record following items.
C0740304 (UMLS CUI-1)
date of onset of COPD exacerbation
Item
Date of Onset
date
C0574845 (UMLS CUI [1,1])
C0740304 (UMLS CUI [1,2])
Item
Outcome
integer
C0085565 (UMLS CUI [1,1])
C0740304 (UMLS CUI [1,2])
CL Item
Resolved (1)
CL Item
Fatal (2)
CL Item
Not resolved (3)
date of resolution or death
Item
Date of Resolution or Death
date
C2985858 (UMLS CUI [1])
C1148348 (UMLS CUI [2])
Item
Severity
integer
C0439793 (UMLS CUI [1,1])
C0740304 (UMLS CUI [1,2])
CL Item
moderate (2)
CL Item
severe (3)
Item
Was the subject withdrawn due to this exacerbation?
text
C0422727 (UMLS CUI [1,1])
C0740304 (UMLS CUI [1,2])
Code List
Was the subject withdrawn due to this exacerbation?
CL Item
Yes (Y)
CL Item
No (N)