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
None reported
Disease State(s) Studied (e.g. acute MI, breast cancer, etc.)
None reported
Study Phase (e.g. Phase I,II,III,IV) Study Phases are defined here
None reported
Study Design (e.g. multicenter, randomized, double blind, placebo controlled)
None reported
Study Arms and How They Were Treated (Intervention) (Explanation here)
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Primary Pre-Specified Endpoint
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Secondary Endpoints
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Inclusion Criteria
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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)
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Commentary, Discussion and Limitations of the Trial (Anyone can add comments)
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Slides
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Video Commentary
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References (How to insert a reference)
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External sites for further information (How to insert links)
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Detailed information about the trial
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)
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Recruitment Status (explanation)
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Enrollment (Total number of patients enrolled)
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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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