Saphenous Vein Graft Disease Clinical Trial
Official title:
Aggressive Cholesterol Therapy to Inhibit Vein Graft Events (ACTIVE Trial): Does High-Dose Postoperative Statin Therapy Improve Graft Patency After Coronary Bypass?
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.
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. ;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT02053909 -
Ticagrelor Antiplatelet Therapy to Reduce Graft Events and Thrombosis
|
Phase 4 | |
Completed |
NCT00263263 -
RRISC Study: Reduction of Restenosis In Saphenous Vein Grafts With Cypher Sirolimus-Eluting Stent.
|
Phase 2 | |
Completed |
NCT01036048 -
A Meta-analysis of Drug Eluting Stents Versus Bare Metal Stents in Saphenous Vein Graft Disease
|
N/A | |
Recruiting |
NCT03175952 -
Virtual Histology Intravascular Ultrasound to Evaluate Prognostic Risks of Saphenous Vein Graft Disease Before Percutaneous Coronary Intervention.
|
N/A | |
Completed |
NCT00453518 -
The RETRIEVE Study: Use of the FiberNet® Embolic Protection System in Saphenous Vein Grafts
|
N/A | |
Terminated |
NCT00264706 -
PolyArginine Treated vEiN grafTs (PATENT)
|
Phase 1/Phase 2 | |
Terminated |
NCT01042444 -
Use of the GARDEX™ Embolic Protection Device During Percutaneous Coronary Interventions of Saphenous Vein Graft
|
N/A |