ID

28156

Beschrijving

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)

Trefwoorden

Versies (5)
  1. 24-09-17 24-09-17 -
  2. 24-09-17 24-09-17 -
  3. 04-10-17 04-10-17 -
  4. 23-10-17 23-10-17 -
  5. 22-12-17 22-12-17 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

22 december 2017

DOI

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Licentie

Creative Commons BY-NC 3.0
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Investigational product Repeating form GSK study Chronic Coronary Heart Disease NCT00799903

Engels

Investigational product Repeating form GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulieren  
Investigational product
Beschrijving

Investigational product

1. Visit
Beschrijving

Visit

Datatype

integer

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

Start Date

Datatype

date

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

Stop Date

Datatype

date

Alias
UMLS CUI [1]
C0806020
Investigational product compliance
Beschrijving

Investigational product compliance

1. Visit
Beschrijving

Visit

Datatype

integer

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

Bottle Code

Datatype

integer

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

Total Number Dispensed

Datatype

integer

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

Total Number Returned

Datatype

integer

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

Total Number Taken

Datatype

integer

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

Investigational product Repeating form GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Investigational product
Item
1. Visit
integer
C0545082 (UMLS CUI [1])
Visit
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])
Visit
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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