ID

28412

Descrição

Study ID: 100601 Clinical Study ID: LPL100601 Study Title: LPL100601, A Clinical Outcomes Study of Darapladib versus Placebo in Subjects with Chronic Coronary Heart Disease to Compare the Incidence of Major Adverse Cardiovascular Events (MACE) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00799903 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: darapladib Trade Name: darapladib Study Indication: Atherosclerosis Study part: Status of treatment blind

Palavras-chave

Versões (4)
  1. 09/10/2017 09/10/2017 -
  2. 16/10/2017 16/10/2017 -
  3. 23/10/2017 23/10/2017 -
  4. 11/01/2018 11/01/2018 -
Titular dos direitos

GlaxoSmithKline

Transferido a

11 de janeiro de 2018

DOI

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Licença

Creative Commons BY-NC 3.0
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Status of treatment blind GSK study Chronic Coronary Heart Disease NCT00799903

Inglês

Status of treatment blind GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulários  
Status of treatment blind
Descrição

Status of treatment blind

1. Was the treatment blind broken during the study?
Descrição

If yes, complete Non-Serious Adverse Events, Serious Adverse Event and/or Investigational Product forms as appropriate

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0749659
UMLS CUI [1,2]
C2347038
If treatment blind was broken, complete the following: Date blind broken
Descrição

Date blind broken

Tipo de dados

date

Alias
UMLS CUI [1]
C0011008
If treatment blind was broken, complete the following: Time blind broken
Descrição

Time blind broken is optional

Tipo de dados

time

Alias
UMLS CUI [1,1]
C3897431
UMLS CUI [1,2]
C0040223
If treatment blind was broken, complete the following: Reason blind broken
Descrição

Reason blind broken

Tipo de dados

text

Alias
UMLS CUI [1]
C3846431
If treatment blind was broken, due to "other" reason, specifiy
Descrição

Reason blind broken other

Tipo de dados

text

Alias
UMLS CUI [1,1]
C3897431
UMLS CUI [1,2]
C0392360
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Similar models

Status of treatment blind GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulários
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
Status of treatment blind
treatment blind broken during the study
Item
1. Was the treatment blind broken during the study?
boolean
C0749659 (UMLS CUI [1,1])
C2347038 (UMLS CUI [1,2])
Date blind broken
Item
If treatment blind was broken, complete the following: Date blind broken
date
C0011008 (UMLS CUI [1])
Time blind broken
Item
If treatment blind was broken, complete the following: Time blind broken
time
C3897431 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Item
If treatment blind was broken, complete the following: Reason blind broken
text
C3846431 (UMLS CUI [1])
Reason blind broken
Code List
If treatment blind was broken, complete the following: Reason blind broken
CL Item
Medical emergency requiring identification of investigational product for further treatment (1)
CL Item
Other (Z)
Item
If treatment blind was broken, due to "other" reason, specifiy
text
C3897431 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
Reason blind broken
Code List
If treatment blind was broken, due to "other" reason, specifiy
CL Item
Medical emergency requiring identification of investigational product for further treatment (1)
CL Item
Other (Z)
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