Informatie:
Fout:
ID
23002
Beschrijving
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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- 19-06-17 19-06-17 -
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19 juni 2017
DOI
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Status of Treatment Blind - GSK Milveterol COPD 100527
Status of Treatment Blind - GSK Milveterol COPD 100527
- StudyEvent: ODM
Similar models
Status of Treatment Blind - GSK Milveterol COPD 100527
- StudyEvent: ODM
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Status of Treatment Blind
C2347038 (UMLS CUI-1)
C0449438 (UMLS CUI-2)
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])
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])
C3897431 (UMLS CUI [1,2])
Item
If 'Yes', reason for subject unblinding:
integer
C0566251 (UMLS CUI [1,1])
C3897431 (UMLS CUI [1,2])
C3897431 (UMLS CUI [1,2])
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])
C0566251 (UMLS CUI [1,2])
C3897431 (UMLS CUI [1,3])