ID

26718

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

Keywords

Versions (4)
  1. 10/9/17 10/9/17 -
  2. 10/16/17 10/16/17 -
  3. 10/23/17 10/23/17 -
  4. 1/11/18 1/11/18 -
Copyright Holder

GlaxoSmithKline

Uploaded on

October 23, 2017

DOI

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License

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

English

Status of treatment blind GSK study Chronic Coronary Heart Disease NCT00799903

1 forms  
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

Data type

boolean

If treatment blind was broken, complete the following: Date blind broken
Description

Date blind broken

Data type

date

If treatment blind was broken, complete the following: Time blind broken
Description

Time blind broken is optional

Data type

time

If treatment blind was broken, complete the following: Reason blind broken
Description

Reason blind broken

Data type

text

If treatment blind was broken, due to "other" reason, specifiy
Description

Reason blind broken other

Data type

text

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Similar models

Status of treatment blind GSK study Chronic Coronary Heart Disease NCT00799903

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Status of treatment blind
treatment blind broken during the study
Item
1. Was the treatment blind broken during the study?
boolean
Date blind broken
Item
If treatment blind was broken, complete the following: Date blind broken
date
Time blind broken
Item
If treatment blind was broken, complete the following: Time blind broken
time
Item
If treatment blind was broken, complete the following: Reason blind broken
text
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
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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