ID

23002

Descripción

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

Palabras clave

Versiones (1)
  1. 19/6/17 19/6/17 -
Subido en

19 de junio de 2017

DOI

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Licencia

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

Inglés

Status of Treatment Blind - GSK Milveterol COPD 100527

1 formularios  
Status of Treatment Blind
Descripción

Status of Treatment Blind

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

blind broken

Tipo de datos

boolean

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

Date of subject unblinding

Tipo de datos

date

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

Reason for subject unblinding

Tipo de datos

integer

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

Specification reason for unblinding

Tipo de datos

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 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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])
Volver a la parte superior de la página 

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