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Action to Control Cardiovascular Risk in Diabetes (ACCORD)
NCT00000620 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to prevent major cardiovascular events (heart attack, stroke, or cardiovascular death) in adults with type 2 diabetes mellitus using intensive glycemic control, intensive blood pressure control, and multiple lipid management.
Conditions Studied
Interventions
- DRUG Anti-hyperglycemic Agents
- DRUG Anti-hypertensive Agents
- DRUG Blinded fenofibrate or placebo plus simvastatin
Study Locations (7)
Minnesota
- Minneapolis Medical Research Foundation — Minneapolis
New York
- Columbia University — New York
North Carolina
- Wake Forest University — Winston-Salem
Ohio
- Case Western Reserve University — Cleveland
Tennessee
- Veterans Affairs — Memphis
Washington
- University of Washington — Seattle
Ontario
- McMaster University — Hamilton
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 10,251 participants |
| Start Date | 1999-09 |
| Est. Completion | 2012-12 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00000620
The ClinicalTrials.gov registry entry for NCT00000620 describes a study currently listed as completed. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 10,251 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is National Heart, Lung, and Blood Institute (NHLBI), which has 381 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 7 conditions, with Hypertension appearing as the primary indexed condition, and to 3 interventions — of which Anti-hyperglycemic Agents is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT00000620 reports 7 study locations spanning 7 distinct geographic areas — top geographies include Minnesota, New York, North Carolina. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT00000620 about?
NCT00000620 is a clinical study titled "Action to Control Cardiovascular Risk in Diabetes (ACCORD)". The purpose of this study is to prevent major cardiovascular events (heart attack, stroke, or cardiovascular death) in adults with type 2 diabetes mellitus using intensive glycemic control, intensive blood pressure control, and multiple lipid management.
What is the current status of trial NCT00000620?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 10,251 participants. The study started on 1999-09. Estimated completion is 2012-12.
What conditions does trial NCT00000620 study?
This clinical trial studies the following conditions: Hypertension, Diabetes Mellitus, Type 2, Cardiovascular Diseases, Diabetes Mellitus, Atherosclerosis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00000620?
The interventions under investigation include: Anti-hyperglycemic Agents (DRUG), Anti-hypertensive Agents (DRUG), Blinded fenofibrate or placebo plus simvastatin (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00000620?
This trial is sponsored by National Heart, Lung, and Blood Institute (NHLBI), which has 381 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00000620 being conducted?
This trial has 7 study locations across Minnesota, New York, North Carolina, Ohio, Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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