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

Keywords

Versions (3)
  1. 9/21/17 9/21/17 -
  2. 10/23/17 10/23/17 -
  3. 12/22/17 12/22/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

December 22, 2017

DOI

To request one please log in.

License

Creative Commons BY-NC 3.0
Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Back to model comments
Itemgroup comments for :

Item comments for :

  • Newest
  • Oldest
  • Popular
  • Newest
    • Newest
    • Oldest
    • Popular

No comments

In order to download data models you must be logged in. Please log in or register for free.

Unscheduled visit GSK study Chronic Coronary Heart Disease NCT00799903

English

Unscheduled visit GSK study Chronic Coronary Heart Disease NCT00799903

1 forms  
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

Data type

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

Data type

boolean

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

date sample taken

Data type

date

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

time sample taken

Data type

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

Data type

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

Data type

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

Data type

text

Alias
UMLS CUI [1]
C1299222
Back to the top of the page

Similar models

Unscheduled visit GSK study Chronic Coronary Heart Disease NCT00799903

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
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])
Back to the top of the page 

Contact

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Help

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial