ID

28153

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: Unscheduled visit

Mots-clés

Versions (3)
  1. 21/09/2017 21/09/2017 -
  2. 23/10/2017 23/10/2017 -
  3. 22/12/2017 22/12/2017 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

22 décembre 2017

DOI

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Licence

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

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Unscheduled visit GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulaires  
Status of visit
Description

Status of visit

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

PK sample collection performed at GSK request for sentinel event

Type de données

integer

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

PK sample collection performed at GSK request for sentinel event

1. Was a pharmacokinetic blood sample obtained?
Description

pharmacokinetic blood sample obtained

Type de données

boolean

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

date sample taken

Type de données

date

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

time sample taken

Type de données

time

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

date of last investigational product dose

Type de données

date

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

time of last investigational product dose

Type de données

time

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

Sample Identifier/Sample Number

Type de données

text

Alias
UMLS CUI [1]
C1299222
Retour au début de la page

Similar models

Unscheduled visit GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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])
Retour au début de la page 

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