ID

28153

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: Unscheduled visit

Palabras clave

Versiones (3)
  1. 21/9/17 21/9/17 -
  2. 23/10/17 23/10/17 -
  3. 22/12/17 22/12/17 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

22 de diciembre de 2017

DOI

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Licencia

Creative Commons BY-NC 3.0
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Unscheduled visit GSK study Chronic Coronary Heart Disease NCT00799903

Inglés

Unscheduled visit GSK study Chronic Coronary Heart Disease NCT00799903

1 formularios  
Status of visit
Descripción

Status of visit

1. Which assessments were performed at this unscheduled visit?
Descripción

PK sample collection performed at GSK request for sentinel event

Tipo de datos

integer

Alias
UMLS CUI [1]
C0220825
PK sample collection performed at GSK request for sentinel event
Descripción

PK sample collection performed at GSK request for sentinel event

1. Was a pharmacokinetic blood sample obtained?
Descripción

pharmacokinetic blood sample obtained

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0031328
UMLS CUI [1,2]
C0178913
If yes, date sample taken
Descripción

date sample taken

Tipo de datos

date

Alias
UMLS CUI [1]
C1302413
if yes, time sample taken
Descripción

time sample taken

Tipo de datos

time

Alias
UMLS CUI [1,1]
C0040223
UMLS CUI [1,2]
C0200345
If Yes, date of last investigational product dose prior to PK sample
Descripción

date of last investigational product dose

Tipo de datos

date

Alias
UMLS CUI [1]
C1762893
If Yes, time of last investigational product dose prior to PK sample
Descripción

time of last investigational product dose

Tipo de datos

time

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0678766
UMLS CUI [1,3]
C0011008
Sample Identifier/Sample Number
Descripción

Sample Identifier/Sample Number

Tipo de datos

text

Alias
UMLS CUI [1]
C1299222
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Similar models

Unscheduled visit GSK study Chronic Coronary Heart Disease NCT00799903

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Status of visit
Item
1. Which assessments were performed at this unscheduled visit?
integer
C0220825 (UMLS CUI [1])
Assessments
Code List
1. Which assessments were performed at this unscheduled visit?
CL Item
Vital signs (1)
C0518766 (UMLS CUI-1)
(Comment:en)
CL Item
ECG (2)
C1623258 (UMLS CUI-1)
(Comment:en)
CL Item
Lab - blood sample (3)
C0005834 (UMLS CUI-1)
(Comment:en)
CL Item
Urine dipstick (4)
C0430370 (UMLS CUI-1)
(Comment:en)
CL Item
PK (5)
C0022877 (UMLS CUI-1)
(Comment:en)
Item Group
PK sample collection performed at GSK request for sentinel event
pharmacokinetic blood sample obtained
Item
1. Was a pharmacokinetic blood sample obtained?
boolean
C0031328 (UMLS CUI [1,1])
C0178913 (UMLS CUI [1,2])
date sample taken
Item
If yes, date sample taken
date
C1302413 (UMLS CUI [1])
time sample taken
Item
if yes, time sample taken
time
C0040223 (UMLS CUI [1,1])
C0200345 (UMLS CUI [1,2])
date of last investigational product dose
Item
If Yes, date of last investigational product dose prior to PK sample
date
C1762893 (UMLS CUI [1])
time of last investigational product dose
Item
If Yes, time of last investigational product dose prior to PK sample
time
C0304229 (UMLS CUI [1,1])
C0678766 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Sample Identifier/Sample Number
Item
Sample Identifier/Sample Number
text
C1299222 (UMLS CUI [1])
Volver a la parte superior de la página 

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