NCT Number: NCT00925717
of PATient Education Related to CV Risk factOrs in Type 2 Diabetes Mellitus(Patrol).
An observational, non-interventional, multi-centre study to provide further information on the utility of test for a predictive marker by investigating the current prevalence of high sensitivity CRP (hs-CRP) testing and characteristics of each CVD risk group.
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Notify MeKey information
Age range
18 year and older
Sex eligibility
All sexes
Study type
Observational
Primary location
Research Site, Cheonan-si, Chungchungnam-do, South Korea
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Subjects who was diagnosed as diabetes
- Subjects who was diagnosed as dyslipidaemia or takes lipid lowering medication
- Clinic visit in the past 6 months more than once
Exclusion criteria
- Subjects who are unwilling or unable to provide their examination and lab result of medical chart.
Treatment and study plan
Primary outcomes
-
Investigate LDL-C goal achievement rate according to ADA recommendation
Time frame: Within the last 6 months from the date of data entry.
Secondary outcomes
-
Investigate reduction of 10-year risk for CHD by using UKPDS risk engine
Time frame: Within the last 6 months from the date of data entry.
Sponsors and collaborators
Lead sponsor
AstraZeneca
Industry
Registry information
Acronym: DART
Important dates
- Study start
- 2009
- Study completion
- 2009
- First posted
- Jun 22, 2009
- Registry last updated
- Jan 26, 2010
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.