ID

24533

Beschrijving

Study ID: 100470 Clinical Study ID: SCO100470 Study Title: A multicentre, randomised, double-blind, parallel group, 24 week study to compare the effect of salmeterol/fluticasone propionate combination product 50/250mcg, with salmeterol 50mcg both delivered twice daily via DISKUS®/ACCUHALER® inhaler on lung function and dyspnoea in subjects with Chronic Obstructive Pulmonary Disease (COPD). Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: N/A Sponsor:GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: fluticasone propionate/salmeterol Trade Name: Serevent Study Indication: Pulmonary Disease, Chronic Obstructive

Trefwoorden

Versies (2)
  1. 05-08-17 05-08-17 -
  2. 08-08-17 08-08-17 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

5 augustus 2017

DOI

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Licentie

Creative Commons BY-NC 3.0
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follow-up salmeterol/fluticasone propionate combination compared to salmeterol on COPD 100470

Engels

follow-up salmeterol/fluticasone propionate combination compared to salmeterol on COPD 100470

1 Formulieren  
OROPHARYNGEAL CANDIDIASIS EXAMINATION
Beschrijving

OROPHARYNGEAL CANDIDIASIS EXAMINATION

Alias
UMLS CUI-1
C0006849
UMLS CUI-2
C0582103
Does the subject have clinical evidence of oropharyngeal candidiasis?
Beschrijving

clinical evidence of oropharyngeal candidiasis

Datatype

text

Alias
UMLS CUI [1,1]
C0006849
UMLS CUI [1,2]
C3887511
Was a swab taken?
Beschrijving

Swab need only be taken if there is clinical evidence of oropharyngeal candidiasis

Datatype

text

Alias
UMLS CUI [1,1]
C0006849
UMLS CUI [1,2]
C0563454
if a swab was taken, result of the swab?
Beschrijving

oropharyngeal candidiasis test result

Datatype

integer

Alias
UMLS CUI [1,1]
C0006849
UMLS CUI [1,2]
C0563454
UMLS CUI [1,3]
C1274040
VITAL SIGNS
Beschrijving

VITAL SIGNS

Alias
UMLS CUI-1
C0518766
Blood pressure
Beschrijving

Position: sitting

Datatype

integer

Maateenheden
  • mmHg
Alias
UMLS CUI [1]
C0005823
mmHg
Heart rate
Beschrijving

heart rate

Datatype

integer

Maateenheden
  • bpm
Alias
UMLS CUI [1]
C0018810
bpm
CENTRAL LABORATORY - BLOOD
Beschrijving

CENTRAL LABORATORY - BLOOD

Alias
UMLS CUI-1
C0018941
Date sample taken
Beschrijving

blood sample taken

Datatype

date

Alias
UMLS CUI [1]
C1277698
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Similar models

follow-up salmeterol/fluticasone propionate combination compared to salmeterol on COPD 100470

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
OROPHARYNGEAL CANDIDIASIS EXAMINATION
C0006849 (UMLS CUI-1)
C0582103 (UMLS CUI-2)
Item
Does the subject have clinical evidence of oropharyngeal candidiasis?
text
C0006849 (UMLS CUI [1,1])
C3887511 (UMLS CUI [1,2])
clinical evidence of oropharyngeal candidiasis
Code List
Does the subject have clinical evidence of oropharyngeal candidiasis?
CL Item
Yes (Y)
CL Item
No (N)
Item
Was a swab taken?
text
C0006849 (UMLS CUI [1,1])
C0563454 (UMLS CUI [1,2])
taking of a swab
Code List
Was a swab taken?
CL Item
Yes (Y)
CL Item
No (N)
Item
if a swab was taken, result of the swab?
integer
C0006849 (UMLS CUI [1,1])
C0563454 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
oropharyngeal candidiasis test result
Code List
if a swab was taken, result of the swab?
CL Item
Negative (1)
CL Item
Positive (2)
CL Item
Not available (4)
Item Group
VITAL SIGNS
C0518766 (UMLS CUI-1)
blood pressure
Item
Blood pressure
integer
C0005823 (UMLS CUI [1])
heart rate
Item
Heart rate
integer
C0018810 (UMLS CUI [1])
Item Group
CENTRAL LABORATORY - BLOOD
C0018941 (UMLS CUI-1)
blood sample taken
Item
Date sample taken
date
C1277698 (UMLS CUI [1])
Terug naar het begin van de pagina 

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