ID
28263
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: New Onset Diabetes Mellitus
Keywords
Versions (4)
- 9/27/17 9/27/17 -
- 10/13/17 10/13/17 -
- 10/23/17 10/23/17 -
- 1/1/18 1/1/18 -
Copyright Holder
GlaxoSmithKline
Uploaded on
January 1, 2018
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.
Itemgroup comments for :
Item comments for :
In order to download data models you must be logged in. Please log in or register for free.
New Onset Diabetes Mellitus GSK study Chronic Coronary Heart Disease NCT00799903
New Onset Diabetes Mellitus GSK study Chronic Coronary Heart Disease NCT00799903
Description
2. Diagnosis based on fasting plasma glucose
Description
Fasting is defined as no caloric intake for at least 8 hours
Data type
text
Alias
- UMLS CUI [1]
- C0583513
Description
FPG results available
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0583513
- UMLS CUI [1,2]
- C0022885
Description
Unit: mg/dL OR mmol/L
Data type
float
Description
Unit FPG results
Data type
text
Alias
- UMLS CUI [1,1]
- C1519795
- UMLS CUI [1,2]
- C0583513
- UMLS CUI [1,3]
- C0022885
Description
3. Diagnosis based on casual plasma glucose
Description
New symptoms of diabetes
Data type
text
Alias
- UMLS CUI [1,1]
- C0037088
- UMLS CUI [1,2]
- C0011849
Description
Casual is defined as any time of day without regard to time since last meal The classic symptoms of hyperglycaemia include polyuria, polydipsia, and unexplained weight loss
Data type
text
Alias
- UMLS CUI [1,1]
- C0202042
- UMLS CUI [1,2]
- C0011900
Description
casual plasma glucose results available
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0430022
- UMLS CUI [1,2]
- C1274040
- UMLS CUI [1,3]
- C0202042
- UMLS CUI [1,4]
- C0011900
Description
Unit: mg/dL OR mmol/L
Data type
float
Alias
- UMLS CUI [1,1]
- C0202042
- UMLS CUI [1,2]
- C0004076
Description
Unit plasma glucose results
Data type
text
Alias
- UMLS CUI [1,1]
- C0202042
- UMLS CUI [1,2]
- C0587081
- UMLS CUI [1,3]
- C1519795
Description
4. Diagnosis based on an oral glucose tolerance test (OGTT)
Description
(The test should be performed as described by World Health Organization, using a glucose load containing the equivalent of 75 g anhydrous glucose dissolved in water)
Data type
text
Alias
- UMLS CUI [1]
- C0029161
Description
OGTT results available
Data type
boolean
Alias
- UMLS CUI [1]
- C0392201
Description
Unit: mg/dL OR mmol/L
Data type
float
Description
Unit OGTT results
Data type
text
Alias
- UMLS CUI [1,1]
- C0392201
- UMLS CUI [1,2]
- C1519795
Description
5. New anti-diabetic medication
Description
6. HbA1c
Description
HbA1c level
Data type
text
Alias
- UMLS CUI [1]
- C0019018
Description
HbA1c results available
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0019018
- UMLS CUI [1,2]
- C0456984
Description
HbA1c results
Data type
float
Measurement units
- %
Alias
- UMLS CUI [1,1]
- C0019018
- UMLS CUI [1,2]
- C1274040
Similar models
New Onset Diabetes Mellitus GSK study Chronic Coronary Heart Disease NCT00799903
C0022885 (UMLS CUI [1,2])
C0583513 (UMLS CUI [1,2])
C0022885 (UMLS CUI [1,3])
(Comment:en)
(Comment:en)
C0011849 (UMLS CUI [1,2])
C0011900 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,2])
C0202042 (UMLS CUI [1,3])
C0011900 (UMLS CUI [1,4])
C0004076 (UMLS CUI [1,2])
C0587081 (UMLS CUI [1,2])
C1519795 (UMLS CUI [1,3])
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
C0456984 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,2])