ID

26718

Descripción

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

Palabras clave

Versiones (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 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

23 de octubre de 2017

DOI

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Licencia

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

Inglés

Status of treatment blind GSK study Chronic Coronary Heart Disease NCT00799903

1 formularios  
Status of treatment blind
Descripción

Status of treatment blind

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

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

Tipo de datos

boolean

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

Date blind broken

Tipo de datos

date

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

Time blind broken is optional

Tipo de datos

time

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

Reason blind broken

Tipo de datos

text

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

Reason blind broken other

Tipo de datos

text

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Similar models

Status of treatment blind GSK study Chronic Coronary Heart Disease NCT00799903

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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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