ID

28412

Description

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

Mots-clés

Versions (4)
  1. 9/10/17 9/10/17 -
  2. 16/10/17 16/10/17 -
  3. 23/10/17 23/10/17 -
  4. 11/1/18 11/1/18 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

11 de enero de 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0
Modèle Commentaires :

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Status of treatment blind GSK study Chronic Coronary Heart Disease NCT00799903

Anglais

Status of treatment blind GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulaires  
Status of treatment blind
Description

Status of treatment blind

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

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

Type de données

boolean

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

Date blind broken

Type de données

date

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

Time blind broken is optional

Type de données

time

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

Reason blind broken

Type de données

text

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

Reason blind broken other

Type de données

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 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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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