ID

23002

Beskrivning

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

Nyckelord

  1. 2017-06-19 2017-06-19 -
Uppladdad den

19 juni 2017

DOI

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Licens

Creative Commons BY-NC 3.0

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Status of Treatment Blind - GSK Milveterol COPD 100527

Status of Treatment Blind - GSK Milveterol COPD 100527

Status of Treatment Blind
Beskrivning

Status of Treatment Blind

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

blind broken

Datatyp

boolean

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

Date of subject unblinding

Datatyp

date

Måttenheter
  • dd.mm.yyyy
Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C3897431
dd.mm.yyyy
If 'Yes', reason for subject unblinding:
Beskrivning

Reason for subject unblinding

Datatyp

integer

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

Specification reason for unblinding

Datatyp

text

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

Similar models

Status of Treatment Blind - GSK Milveterol COPD 100527

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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])
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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