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Stroke Interventions in Clinical Trials
Printable Version
ACCORD
Action to Control Cardiovascular Risk in Diabetes



Principal Investigator
Robert Byington, PhD

Contact Email
bbyingto@wfubmc.edu

Sponsor



Trial Phase:Phase III
Study Size Planned:10000
Centers Planned:70
Max Age:79
Min Age:40
Follow-up Duration:6 Years
ISRCTN#NCT00000620
Status:
This study is ongoing, but not recruiting participants.

Purpose:
To evaluate 3 complementary medical treatment strategies for type 2 diabetes to enhance the options for reducing the very high rate of major Cardiovascular Disease (CVD) morbidity and mortality.

Location(s):
United States, Canada

Year Started: 1999

Design:
A randomized, multicenter, double 2 X 2 factorial design.

Inclusion Criteria
Patients 40 years or olders with a history of clinical cardiovascular disease or patients 55 years or older without a history of clinical cardiovascular disease but considered at high risk of CVD event diagnosed with Type 2 diabetes.

Exclusion Criteria
Patients who have conditions that will reduce the safety or benefits of the ACCORD procedures. Patients who are not able to follow ACCORD procedures of taking the prescribed medications, going to clinic visits, and following health tips given.

Patient Involvement:
Patients will be randomly assigned to either a standard or aggressive control of blood sugar, then based on their blood pressure and cholesterol levels, assigned to one of the other two groups.

Primary Outcome:
Lowered risk of CVD in each of the 3 medical treatment strategies: lowered blood sugar, lowered blood pressure (<120mmHg systolic), blood fats (lower LDL and increase HDL).

Secondary Outcome:
Total mortality.

Source of Information:
Press. ACCORD Website.
ClinicalTrials.gov

Web Links and Publications:
ACCORD Trial Website

Effects of intensive glucose lowering in type 2 diabetes.
N Engl J Med 2008 Jun 12;358(24):2545-59

Rationale, design, and methods of the Action to Control Cardiovascular Risk in Diabetes Eye Study (ACCORD-EYE).
Am J Cardiol 2007 Jun 18;99(12A):103i-111i

Action to Control Cardiovascular Risk in Diabetes (ACCORD) trial: design and methods.
Am J Cardiol 2007 Jun 18;99(12A):21i-33i

Glycemia treatment strategies in the Action to Control Cardiovascular Risk in Diabetes (ACCORD) trial.
Am J Cardiol 2007 Jun 18;99(12A):34i-43i

Prevention of cardiovascular disease in persons with type 2 diabetes mellitus: current knowledge and rationale for the Action to Control Cardiovascular Risk in Diabetes (ACCORD) trial.
Am J Cardiol 2007 Jun 18;99(12A):4i-20i

Evolution of the lipid trial protocol of the Action to Control Cardiovascular Risk in Diabetes (ACCORD) trial.
Am J Cardiol 2007 Jun 18;99(12A):56i-67i

Recruitment strategies in the Action to Control Cardiovascular Risk in Diabetes (ACCORD) trial.
Am J Cardiol 2007 Jun 18;99(12A):68i-79i

Severe hypoglycemia monitoring and risk management procedures in the Action to Control Cardiovascular Risk in Diabetes (ACCORD) trial.
Am J Cardiol 2007 Jun 18;99(12A):80i-89i

Health-related quality of life and cost-effectiveness components of the Action to Control Cardiovascular Risk in Diabetes (ACCORD) trial: rationale and design.
Am J Cardiol 2007 Jun 18;99(12A):90i-102i

The Action to Control Cardiovascular Risk in Diabetes Memory in Diabetes Study (ACCORD-MIND): rationale, design, and methods.
Am J Cardiol 2007 Jun 18;99(12A):112i-122i

Rationale and design for the blood pressure intervention of the Action to Control Cardiovascular Risk in Diabetes (ACCORD) trial.
Am J Cardiol 2007 Jun 18;99(12A):44i-55i

Action to Control Cardiovascular Risk in Diabetes
ClinicalTrials.gov

This information last updated on: 12/30/2008

Reviewed on: 06/19/2009.

UID: 510

   

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