ID

23002

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

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Creative Commons BY-NC 3.0
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Status of Treatment Blind - GSK Milveterol COPD 100527

Anglais

Status of Treatment Blind - GSK Milveterol COPD 100527

1 Formulaires  
Status of Treatment Blind
Description

Status of Treatment Blind

Alias
UMLS CUI-1
C2347038
UMLS CUI-2
C0449438
Was the treatment blind for this subject broken during the study?
Description

blind broken

Type de données

boolean

Alias
UMLS CUI [1,1]
C3897431
UMLS CUI [1,2]
C2347038
lf 'Yes', date of subject unblinding:
Description

Date of subject unblinding

Type de données

date

Unités de mesure
  • dd.mm.yyyy
Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C3897431
dd.mm.yyyy
If 'Yes', reason for subject unblinding:
Description

Reason for subject unblinding

Type de données

integer

Alias
UMLS CUI [1,1]
C0566251
UMLS CUI [1,2]
C3897431
If 'Other', please specify:
Description

Specification reason for unblinding

Type de données

text

Alias
UMLS CUI [1,1]
C2348235
UMLS CUI [1,2]
C0566251
UMLS CUI [1,3]
C3897431
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Similar models

Status of Treatment Blind - GSK Milveterol COPD 100527

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Status of Treatment Blind
C2347038 (UMLS CUI-1)
C0449438 (UMLS CUI-2)
blind broken
Item
Was the treatment blind for this subject broken during the study?
boolean
C3897431 (UMLS CUI [1,1])
C2347038 (UMLS CUI [1,2])
Date of subject unblinding
Item
lf 'Yes', date of subject unblinding:
date
C0011008 (UMLS CUI [1,1])
C3897431 (UMLS CUI [1,2])
Item
If 'Yes', reason for subject unblinding:
integer
C0566251 (UMLS CUI [1,1])
C3897431 (UMLS CUI [1,2])
Reason for subject unblinding
Code List
If 'Yes', reason for subject unblinding:
CL Item
Medical emergency requiring identity of investigational product for further treatment (1)
CL Item
Other (please specify below) (2)
Specification reason for unblinding
Item
If 'Other', please specify:
text
C2348235 (UMLS CUI [1,1])
C0566251 (UMLS CUI [1,2])
C3897431 (UMLS CUI [1,3])
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