Action To Control Cardiovascular Risk In Diabetes

Complete Title of Study

Action to Control Cardiovascular Risk in Diabetes (ACCORD)

Study Acronym (The trial's abbreviation if there is one)

ACCORD

Principal Investigator, Co-investigators, and Collaborating Institutions

Study Director: Denise Simons-Morton, MD, PhD of the National Heart, Lung, and Blood Institute (NHLBI)
Study Chair: William Friedewald, MD of Columbia University, New York, NY
Principal Investigator:Robert Byington, PhD of Wake Forest University, Winston-Salem, NC

Overview of Trial

The goal of the ACCORD study was to evaluate the ability of intensive glycemic control, intensive blood pressure control, and multiple lipid management to prevent major cardiovascular events in 10,251 type 2 diabetes patients.

Disease State(s) Studied (e.g. acute MI, breast cancer, etc.)

• Atherosclerosis
• Cardiovascular Diseases
• Hypercholesterolemia
• Hypertension
• Diabetes Mellitus, Type 2
• Coronary Disease

Study Phase (e.g. Phase I,II,III,IV) Study Phases are defined here

Phase III

Study Design (e.g. multicenter, randomized, double blind, placebo controlled)

Prevention, Randomized, Open Label, Active Control, Factorial Assignment, Efficacy Study

Study Arms and How They Were Treated (Intervention) (Explanation here)

• Experimental: A strategy of intensive glycemia treatment to HbA1 less than 6%
• Active Comparator: A strategy of multiple drugs to treat HbA1c to 7.0%-7.9%

Experimental: A strategy of BP treatment for SBP less than 120 mm Hg Active Comparator: A strategy of BP treatment for SBP less than 140 mm Hg Experimental: Blinded fenofibrate + simvastatin 20-40 mg/d

Primary Pre-Specified Endpoint

None reported

Secondary Endpoints

None reported

Inclusion Criteria

None reported

Exclusion Criteria

None reported

Outcome: Primary endpoint (Report both relative risk reduction and absolute risk reduction as well as number needed to treat if available)

None reported

Outcome: Secondary endpoint (Report both relative risk reduction and absolute risk reduction as well as number needed to treat if available)

None reported

Outcome: Exploratory endpoints (Report both relative risk reduction and absolute risk reduction as well as number needed to treat if available)

None reported

Outcome: Safety endpoints (Report both relative risk and absolute risk as well as number needed to harm if available)

None reported

Conclusions of the Investigators (Quote the investigators conclusions here)

None reported

Commentary, Discussion and Limitations of the Trial (Anyone can add comments)

None reported

Slides

None reported

Video Commentary

None reported

References (How to insert a reference)

None reported

External sites for further information (How to insert links)

None reported

Ages

__ years to ___ years

Gender (Indicate whether men, women or both were enrolled)

None reported

Accepts Healthy Volunteers (Answer yes or no)

None reported

Enrollment Period (Study start and end date)

None reported

Recruitment Status (explanation)

None reported

Enrollment (Total number of patients enrolled)

None reported

Study Sponsor (e.g. Investigator initiated or company name)

None reported (this may not have yet been ascertained)

Source of Data (Where is this data on this page coming from: publication, principal investigator, or co-investigator)

None reported

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