ID

23007

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

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  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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End of Study Record - GSK Milveterol COPD 100527

Anglais

End of Study Record - GSK Milveterol COPD 100527

1 Formulaires  
End of Study Record
Description

End of Study Record

Alias
UMLS CUI-1
C0008976
UMLS CUI-2
C0444930
Date of subject completion or discontinuation from the study
Description

Date of subject completion or discontinuation from the study

Type de données

date

Unités de mesure
  • dd.mm.yyyy
Alias
UMLS CUI [1,1]
C2348577
UMLS CUI [1,2]
C0011008
dd.mm.yyyy
Time of subject completion or discontinuation from the study
Description

Time of subject completion or discontinuation from the study

Type de données

time

Unités de mesure
  • hh:mm
Alias
UMLS CUI [1,1]
C2348577
UMLS CUI [1,2]
C0040223
hh:mm
Did the subject discontinue the study prematurely?
Description

premature discontinuation of study

Type de données

boolean

Alias
UMLS CUI [1,1]
C2348577
UMLS CUI [1,2]
C1279919
If 'Yes', the primary reason for discontinuation:
Description

Reason for premature discontinuation

Type de données

integer

Alias
UMLS CUI [1,1]
C0566251
UMLS CUI [1,2]
C2348577
UMLS CUI [1,3]
C1279919
If 'Other', please specify:
Description

Specification reason for discontinuation

Type de données

text

Alias
UMLS CUI [1,1]
C2348235
UMLS CUI [1,2]
C0566251
UMLS CUI [1,3]
C2348577
UMLS CUI [1,4]
C1279919
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Similar models

End of Study Record - GSK Milveterol COPD 100527

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
End of Study Record
C0008976 (UMLS CUI-1)
C0444930 (UMLS CUI-2)
Date of subject completion or discontinuation from the study
Item
Date of subject completion or discontinuation from the study
date
C2348577 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Time of subject completion or discontinuation from the study
Item
Time of subject completion or discontinuation from the study
time
C2348577 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
premature discontinuation of study
Item
Did the subject discontinue the study prematurely?
boolean
C2348577 (UMLS CUI [1,1])
C1279919 (UMLS CUI [1,2])
Item
If 'Yes', the primary reason for discontinuation:
integer
C0566251 (UMLS CUI [1,1])
C2348577 (UMLS CUI [1,2])
C1279919 (UMLS CUI [1,3])
Reason for premature discontinuation
Code List
If 'Yes', the primary reason for discontinuation:
CL Item
Adverse event (1)
CL Item
Consent withdrawn (2)
CL Item
Lost to follow up (3)
CL Item
Protocol violation (4)
CL Item
Other (please specify below) (5)
Specification reason for discontinuation
Item
If 'Other', please specify:
text
C2348235 (UMLS CUI [1,1])
C0566251 (UMLS CUI [1,2])
C2348577 (UMLS CUI [1,3])
C1279919 (UMLS CUI [1,4])
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