Aggressive Cholesterol Therapy to Inhibit Vein Graft Events After CABG (ACTIVE Trial)
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Purpose
During coronary artery bypass graft surgery (CABG), saphenous vein from the leg is used to bypass the atherosclerotic blockages in the arteries of the heart. Unfortunately, vein bypasses themselves develop blockages over time, a process termed saphenous vein graft disease. By lowering cholesterol levels in the blood, statin medications are used after surgery to prevent the development of atherosclerotic blockages in the vein bypasses. Recently, higher doses of statin medications have been introduced, with some studies showing that they are more effective than traditional doses when used in heart attack patients. Furthermore, laboratory tests have shown that higher doses of statin medications can slow the development of atherosclerosis. Despite these benefits, very little is known regarding the use of high-dose statin therapy after bypass surgery in humans.
The goal of this study will be to see if high-dose statin therapy will prevent the development of vein graft occlusion during the first year after bypass surgery. Patients will be randomized to receive either high-dose statin therapy or conventional moderate-dose statin therapy starting within 4 days of surgery and continuing for the duration of one year after the operation. The statin medication will be given in capsule form. During the course of this study, neither the patient nor the health care team will know which treatment each patient is receiving. One year after bypass surgery, a computed tomography (CT) coronary angiogram will be performed to evaluate the patency of the vein bypasses.
| Condition | Intervention | Phase |
|---|---|---|
|
Saphenous Vein Graft Disease |
Drug: Atorvastatin 80 mg daily Drug: Atorvastatin 10 mg daily |
Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor) Primary Purpose: Prevention |
| Official Title: | Aggressive Cholesterol Therapy to Inhibit Vein Graft Events (ACTIVE Trial): Does High-Dose Postoperative Statin Therapy Improve Graft Patency After Coronary Bypass? |
- Saphenous vein graft patency [ Time Frame: 1 year after CABG ] [ Designated as safety issue: No ]Vein graft patency will be assessed in a blinded fashion by CT coronary angiography 1 year after CABG
- Safety of high-dose statin therapy early after CABG [ Time Frame: Within 1 year after CABG ] [ Designated as safety issue: Yes ]Safety measures will include the incidence of major adverse cardiovascular events (mortality, myocardial infarction, cerebrovascular accident, hospitalization for coronary ischemia, and need for coronary intervention), the incidence of elevations in liver enzyme levels, the incidence of myopathy, and the incidence of rhabdomyolysis.
| Estimated Enrollment: | 200 |
| Study Start Date: | March 2012 |
| Estimated Study Completion Date: | March 2014 |
| Estimated Primary Completion Date: | March 2014 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: High-dose statin therapy
Atorvastatin 80 mg daily
|
Drug: Atorvastatin 80 mg daily
Atorvastatin 80 mg daily for 1 year
|
|
Active Comparator: Moderate-dose statin therapy
Atorvastatin 10 mg daily
|
Drug: Atorvastatin 10 mg daily
Atorvastatin 10 mg daily for 1 year
|
Detailed Description:
The current clinical guidelines recommend treatment to achieve LDL levels <100 mg/dL after surgical coronary revascularization. However, recent studies have illustrated that even more intensive lipid reduction with high-dose statins can further improve cardiovascular outcomes. Targeting LDL levels to 70 mg/dL after CABG with intensive statin therapy may prevent the process of postoperative saphenous vein graft disease and lead to improved graft patency. Therefore, in the ACTIVE Trial, we will conduct a randomized controlled trial comparing high-dose (80 mg atorvastatin) to moderate-dose (10 mg atorvastatin)statin therapy in patients undergoing CABG with saphenous vein grafts. The effect of aggressive cholesterol therapy on the process of vein graft disease will be examined with computed tomography (CT) coronary angiography one year after CABG. This study will address the subject of postoperative high-dose statin therapy and help determine the optimal lipid-lowering strategy following CABG.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Patients undergoing first-time CABG with at least 1 saphenous vein graft
Exclusion Criteria:
- Redo-CABG
- Statin allergy
- Severe renal dysfunction
- Severe liver disease
Contacts and Locations| Contact: Alexander Kulik, MD MPH | 561-955-6300 | alex_kulik@yahoo.com |
| United States, Florida | |
| Lynn Heart and Vascular Institute, Boca Raton Regional Hospital | Recruiting |
| Boca Raton, Florida, United States, 33486 | |
| Contact: Alexander Kulik, MD MPH 561-955-6300 alex_kulik@yahoo.com | |
| Principal Investigator: Alexander Kulik, MD MPH | |
| Principal Investigator: | Alexander Kulik, MD MPH | Lynn Heart and Vascular Institute, Boca Raton Regional Hospital |
More Information
Publications:
| Responsible Party: | Dr. Alexander Kulik, Cardiovascular Surgeon, Boca Raton Regional Hospital |
| ClinicalTrials.gov Identifier: | NCT01528709 History of Changes |
| Other Study ID Numbers: | 2011.02 |
| Study First Received: | February 6, 2012 |
| Last Updated: | December 12, 2012 |
| Health Authority: | United States: Western Institutional Review Board United States: Food and Drug Administration |
Keywords provided by Boca Raton Regional Hospital:
|
Statin, CABG, saphenous vein graft, graft occlusion, lipids |
Additional relevant MeSH terms:
|
Atorvastatin Hydroxymethylglutaryl-CoA Reductase Inhibitors Anticholesteremic Agents Hypolipidemic Agents Antimetabolites |
Molecular Mechanisms of Pharmacological Action Pharmacologic Actions Enzyme Inhibitors Lipid Regulating Agents Therapeutic Uses |
ClinicalTrials.gov processed this record on May 23, 2013