ID

23004

Description

Study ID: 100527 Clinical Study ID: B2E100527 Study Title: A randomised, double blind, placebo controlled, parellel group study to examine the efficacy, safety, tolerability and systemic pharmacokinetic profile of repeated inhaled doses of GSK159797 Sponsor: GlaxoSmithKline Phase: phase 2 Study Recruitment Status: Completed Generic Name: milveterol Trade Name: Milveterol Study Indication: Pulmonary Disease, Chronic Obstructive

Mots-clés

Versions (1)
  1. 19/06/2017 19/06/2017 -
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19 juin 2017

DOI

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Creative Commons BY-NC 3.0
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Concomitant Medications - GSK Milveterol COPD 100527

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Concomitant Medications - GSK Milveterol COPD 100527

1 Formulaires  
Concomitant Medications
Description

Concomitant Medications

Alias
UMLS CUI-1
C1704627
Were any concomitant medications taken by the subject during the study?
Description

concomitant medications during study

Type de données

boolean

Alias
UMLS CUI [1]
C1707479
Drug (Trade name preferred)
Description

Drug Name

Type de données

text

Alias
UMLS CUI [1]
C2347852
Dose
Description

Dose

Type de données

float

Alias
UMLS CUI [1]
C2826638
Unit
Description

Unit

Type de données

text

Alias
UMLS CUI [1]
C2826646
Frequency
Description

Frequency

Type de données

text

Alias
UMLS CUI [1]
C2826654
Route
Description

Route

Type de données

text

Alias
UMLS CUI [1]
C2826730
Date started
Description

Start Date

Type de données

date

Unités de mesure
  • dd.mm.yyyy
Alias
UMLS CUI [1]
C2826734
dd.mm.yyyy
Started pre-study
Description

Started pre-study

Type de données

boolean

Alias
UMLS CUI [1]
C2981448
Start time
Description

Start time

Type de données

time

Unités de mesure
  • hh:mm
Alias
UMLS CUI [1]
C2826740
hh:mm
Date stopped
Description

Stop Date

Type de données

date

Unités de mesure
  • dd.mm.yyyy
Alias
UMLS CUI [1]
C2826744
dd.mm.yyyy
Medication continued post-study
Description

Ongoing Medication

Type de données

boolean

Alias
UMLS CUI [1]
C2826666
End time
Description

End time

Type de données

time

Unités de mesure
  • hh:mm
Alias
UMLS CUI [1]
C2826659
hh:mm
Conditions treated/indication
Description

Reason for Medication

Type de données

text

Alias
UMLS CUI [1]
C2826696
Was drug administered for an adverse event?
Description

drug administered for an adverse event

Type de données

boolean

Alias
UMLS CUI [1,1]
C2826696
UMLS CUI [1,2]
C0877248
Retour au début de la page

Similar models

Concomitant Medications - GSK Milveterol COPD 100527

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Concomitant Medications
C1704627 (UMLS CUI-1)
concomitant medications during study
Item
Were any concomitant medications taken by the subject during the study?
boolean
C1707479 (UMLS CUI [1])
Drug Name
Item
Drug (Trade name preferred)
text
C2347852 (UMLS CUI [1])
Dose
Item
Dose
float
C2826638 (UMLS CUI [1])
Unit
Item
Unit
text
C2826646 (UMLS CUI [1])
Frequency
Item
Frequency
text
C2826654 (UMLS CUI [1])
Route
Item
Route
text
C2826730 (UMLS CUI [1])
Start Date
Item
Date started
date
C2826734 (UMLS CUI [1])
Started pre-study
Item
Started pre-study
boolean
C2981448 (UMLS CUI [1])
Start time
Item
Start time
time
C2826740 (UMLS CUI [1])
Stop Date
Item
Date stopped
date
C2826744 (UMLS CUI [1])
Ongoing Medication
Item
Medication continued post-study
boolean
C2826666 (UMLS CUI [1])
End time
Item
End time
time
C2826659 (UMLS CUI [1])
Reason for Medication
Item
Conditions treated/indication
text
C2826696 (UMLS CUI [1])
drug administered for an adverse event
Item
Was drug administered for an adverse event?
boolean
C2826696 (UMLS CUI [1,1])
C0877248 (UMLS CUI [1,2])
Retour au début de la page 

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