ID

28156

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: Investigational product Repeating form (Scheduled visits)

Keywords

  1. 9/24/17 9/24/17 -
  2. 9/24/17 9/24/17 -
  3. 10/4/17 10/4/17 -
  4. 10/23/17 10/23/17 -
  5. 12/22/17 12/22/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

December 22, 2017

DOI

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License

Creative Commons BY-NC 3.0

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Investigational product Repeating form GSK study Chronic Coronary Heart Disease NCT00799903

Investigational product Repeating form GSK study Chronic Coronary Heart Disease NCT00799903

Investigational product
Description

Investigational product

1. Visit
Description

Visit

Data type

integer

Alias
UMLS CUI [1]
C0545082
2. Start Date
Description

Start Date

Data type

date

Alias
UMLS CUI [1]
C0808070
3. Stop Date
Description

Stop Date

Data type

date

Alias
UMLS CUI [1]
C0806020
Investigational product compliance
Description

Investigational product compliance

1. Visit
Description

Visit

Data type

integer

Alias
UMLS CUI [1]
C0545082
2. Bottle Code
Description

Bottle Code

Data type

integer

Alias
UMLS CUI [1]
C0179376
3. Total Number Dispensed
Description

Total Number Dispensed

Data type

integer

Alias
UMLS CUI [1]
C0805077
4. Total Number Returned
Description

Total Number Returned

Data type

integer

Alias
UMLS CUI [1,1]
C2699071
UMLS CUI [1,2]
C0039225
5. Total Number Taken
Description

Total Number Taken

Data type

integer

Alias
UMLS CUI [1,1]
C0039225
UMLS CUI [1,2]
C1883727

Similar models

Investigational product Repeating form GSK study Chronic Coronary Heart Disease NCT00799903

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Investigational product
Item
1. Visit
integer
C0545082 (UMLS CUI [1])
Code List
1. Visit
CL Item
Baseline (0)
CL Item
Month 1 (1)
CL Item
Month 3 (3)
CL Item
Month 6 (6)
CL Item
Month 12 (12)
CL Item
Month 18 (18)
CL Item
Month 24 (24)
CL Item
Month 30 (30)
CL Item
Month 36 (36)
CL Item
Month 42 (42)
CL Item
Month 48 (48)
CL Item
Month 54 (54)
CL Item
Month 60 (60)
CL Item
Month 66 (66)
CL Item
Month 72 (72)
Start Date
Item
2. Start Date
date
C0808070 (UMLS CUI [1])
Stop Date
Item
3. Stop Date
date
C0806020 (UMLS CUI [1])
Item Group
Investigational product compliance
Item
1. Visit
integer
C0545082 (UMLS CUI [1])
Code List
1. Visit
CL Item
Baseline (0)
CL Item
Month 1 (1)
CL Item
Month 3 (3)
CL Item
Month 6 (6)
CL Item
Month 12 (12)
CL Item
Month 18 (18)
CL Item
Month 24 (24)
CL Item
Month 30 (30)
CL Item
Month 36 (36)
CL Item
Month 42 (42)
CL Item
Month 48 (48)
CL Item
Month 54 (54)
CL Item
Month 60 (60)
CL Item
Month 66 (66)
CL Item
Month 72 (72)
Bottle Code
Item
2. Bottle Code
integer
C0179376 (UMLS CUI [1])
Total Number Dispensed
Item
3. Total Number Dispensed
integer
C0805077 (UMLS CUI [1])
Total Number Returned
Item
4. Total Number Returned
integer
C2699071 (UMLS CUI [1,1])
C0039225 (UMLS CUI [1,2])
Total Number Taken
Item
5. Total Number Taken
integer
C0039225 (UMLS CUI [1,1])
C1883727 (UMLS CUI [1,2])

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