ID

26257

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

Mots-clés

  1. 27/09/2017 27/09/2017 -
  2. 13/10/2017 13/10/2017 -
  3. 23/10/2017 23/10/2017 -
  4. 01/01/2018 01/01/2018 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

13 octobre 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

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New Onset Diabetes Mellitus GSK study Chronic Coronary Heart Disease NCT00799903

New Onset Diabetes Mellitus GSK study Chronic Coronary Heart Disease NCT00799903

New Onset Diabetes Mellitus, Date of diagnosis
Description

New Onset Diabetes Mellitus, Date of diagnosis

1. Date of diagnosis
Description

Date of diagnosis

Type de données

date

2. Diagnosis based on fasting plasma glucose
Description

2. Diagnosis based on fasting plasma glucose

Diagnosis based on fasting plasma glucose >= 126 mg/dL (7 mmol/L)?
Description

Fasting is defined as no caloric intake for at least 8 hours

Type de données

text

If yes, are FPG results available?
Description

FPG results available

Type de données

boolean

IF FPG results available, record the results below
Description

Unit: mg/dL OR mmol/L

Type de données

float

Unit FPG results
Description

Unit FPG results

Type de données

text

3. Diagnosis based on casual plasma glucose
Description

3. Diagnosis based on casual plasma glucose

New symptoms of diabetes?
Description

New symptoms of diabetes

Type de données

text

3. Diagnosis based on casual plasma glucose >= 200 mg/dL (11.1 mmol/L)?
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

Type de données

text

If Yes, are casual plasma glucose results available?
Description

casual plasma glucose results available

Type de données

boolean

If casual plasma glucose results available, record the results below
Description

Unit: mg/dL OR mmol/L

Type de données

float

Unit: plasma glucose results
Description

Unit plasma glucose results

Type de données

text

4. Diagnosis based on an oral glucose tolerance test (OGTT)
Description

4. Diagnosis based on an oral glucose tolerance test (OGTT)

Diagnosis based on an oral glucose tolerance test (OGTT) 2-hour post load glucose >=200 mg/dL (11.1 mmol/L)?
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)

Type de données

text

If Yes, are OGTT results available?
Description

OGTT results available

Type de données

boolean

If OGTT results available, record the results below
Description

Unit: mg/dL OR mmol/L

Type de données

float

Unit: OGTT results
Description

Unit OGTT results

Type de données

text

5. New anti-diabetic medication
Description

5. New anti-diabetic medication

Did the subject start new anti-diabetic medication?
Description

new anti-diabetic medication

Type de données

text

6. HbA1c
Description

6. HbA1c

Did the subject have HbA1c >= 6.5%?
Description

HbA1c level

Type de données

text

If Yes, are HbA1c results available?
Description

HbA1c results available

Type de données

boolean

If HbA1c results available, record the results below
Description

HbA1c results

Type de données

float

Unités de mesure
  • %
%

Similar models

New Onset Diabetes Mellitus GSK study Chronic Coronary Heart Disease NCT00799903

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
New Onset Diabetes Mellitus, Date of diagnosis
Date of diagnosis
Item
1. Date of diagnosis
date
Item Group
2. Diagnosis based on fasting plasma glucose
Item
Diagnosis based on fasting plasma glucose >= 126 mg/dL (7 mmol/L)?
text
Code List
Diagnosis based on fasting plasma glucose >= 126 mg/dL (7 mmol/L)?
CL Item
Unknown (U)
CL Item
No (N)
CL Item
Yes (Y)
FPG results available
Item
If yes, are FPG results available?
boolean
FPG results
Item
IF FPG results available, record the results below
float
Item
Unit FPG results
text
Code List
Unit FPG results
CL Item
mg/dL (mg/dL)
CL Item
mmol/L (mmol/L)
Item Group
3. Diagnosis based on casual plasma glucose
Item
New symptoms of diabetes?
text
Code List
New symptoms of diabetes?
CL Item
Unknown (U)
CL Item
Yes (Y)
CL Item
No (N)
Item
3. Diagnosis based on casual plasma glucose >= 200 mg/dL (11.1 mmol/L)?
text
Code List
3. Diagnosis based on casual plasma glucose >= 200 mg/dL (11.1 mmol/L)?
CL Item
Unknown (U)
CL Item
Yes (Y)
CL Item
No (N)
casual plasma glucose results available
Item
If Yes, are casual plasma glucose results available?
boolean
plasma glucose results
Item
If casual plasma glucose results available, record the results below
float
Item
Unit: plasma glucose results
text
Code List
Unit: plasma glucose results
CL Item
mg/dL (mg/dL)
CL Item
mmol/L (mmol/L)
Item Group
4. Diagnosis based on an oral glucose tolerance test (OGTT)
Item
Diagnosis based on an oral glucose tolerance test (OGTT) 2-hour post load glucose >=200 mg/dL (11.1 mmol/L)?
text
Code List
Diagnosis based on an oral glucose tolerance test (OGTT) 2-hour post load glucose >=200 mg/dL (11.1 mmol/L)?
CL Item
Unknown (U)
CL Item
No (N)
CL Item
Yes (Y)
OGTT results available
Item
If Yes, are OGTT results available?
boolean
OGTT results
Item
If OGTT results available, record the results below
float
Item
Unit: OGTT results
text
Code List
Unit: OGTT results
CL Item
mg/dL (mg/dL)
CL Item
mmol/L (mmol/L)
Item Group
5. New anti-diabetic medication
Item
Did the subject start new anti-diabetic medication?
text
Code List
Did the subject start new anti-diabetic medication?
CL Item
Unknown (U)
CL Item
Yes (record details of medication in the Concomitant Medication form) (Y)
CL Item
No (N)
Item Group
6. HbA1c
Item
Did the subject have HbA1c >= 6.5%?
text
Code List
Did the subject have HbA1c >= 6.5%?
CL Item
Unknown (U)
CL Item
No (N)
CL Item
Yes (Y)
HbA1c results available
Item
If Yes, are HbA1c results available?
boolean
HbA1c results
Item
If HbA1c results available, record the results below
float

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