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Aggressive Cholesterol Therapy to Inhibit Vein Graft Events After CABG (ACTIVE Trial) (ACTIVE)

Primary Purpose

Saphenous Vein Graft Disease

Status
Completed
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
Atorvastatin 80 mg daily
Atorvastatin 10 mg daily
Sponsored by
Boca Raton Regional Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Saphenous Vein Graft Disease focused on measuring Statin,, CABG,, saphenous vein graft,, graft occlusion,, lipids

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Lynn Heart and Vascular Institute, Boca Raton Regional Hospital
  • University of Ottawa Heart Institute

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

High-dose statin therapy

Moderate-dose statin therapy

Arm Description

Atorvastatin 80 mg daily

Atorvastatin 10 mg daily

Outcomes

Primary Outcome Measures

Saphenous Vein Graft Occlusion (Percentage of Vein Grafts Occluded) Based on CT Coronary Angiography at 1 Year
Vein graft patency will be assessed in a blinded fashion by CT coronary angiography 1 year after CABG

Secondary Outcome Measures

Vein Graft Stenosis 1 Year After CABG Based on CT Coronary Angiography
Vein graft stenosis 1 year after CABG based on CT coronary angiography

Full Information

First Posted
February 6, 2012
Last Updated
September 6, 2018
Sponsor
Boca Raton Regional Hospital
Collaborators
Pfizer
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1. Study Identification

Unique Protocol Identification Number
NCT01528709
Brief Title
Aggressive Cholesterol Therapy to Inhibit Vein Graft Events After CABG (ACTIVE Trial)
Acronym
ACTIVE
Official Title
Aggressive Cholesterol Therapy to Inhibit Vein Graft Events (ACTIVE Trial): Does High-Dose Postoperative Statin Therapy Improve Graft Patency After Coronary Bypass?
Study Type
Interventional

2. Study Status

Record Verification Date
September 2018
Overall Recruitment Status
Completed
Study Start Date
March 2012 (undefined)
Primary Completion Date
January 2017 (Actual)
Study Completion Date
January 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Boca Raton Regional Hospital
Collaborators
Pfizer

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Saphenous Vein Graft Disease
Keywords
Statin,, CABG,, saphenous vein graft,, graft occlusion,, lipids

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
173 (Actual)

8. Arms, Groups, and Interventions

Arm Title
High-dose statin therapy
Arm Type
Experimental
Arm Description
Atorvastatin 80 mg daily
Arm Title
Moderate-dose statin therapy
Arm Type
Active Comparator
Arm Description
Atorvastatin 10 mg daily
Intervention Type
Drug
Intervention Name(s)
Atorvastatin 80 mg daily
Intervention Description
Atorvastatin 80 mg daily for 1 year
Intervention Type
Drug
Intervention Name(s)
Atorvastatin 10 mg daily
Intervention Description
Atorvastatin 10 mg daily for 1 year
Primary Outcome Measure Information:
Title
Saphenous Vein Graft Occlusion (Percentage of Vein Grafts Occluded) Based on CT Coronary Angiography at 1 Year
Description
Vein graft patency will be assessed in a blinded fashion by CT coronary angiography 1 year after CABG
Time Frame
1 year after CABG
Secondary Outcome Measure Information:
Title
Vein Graft Stenosis 1 Year After CABG Based on CT Coronary Angiography
Description
Vein graft stenosis 1 year after CABG based on CT coronary angiography
Time Frame
Within 1 year after CABG

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alexander Kulik, MD MPH
Organizational Affiliation
Lynn Heart and Vascular Institute, Boca Raton Regional Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Marc Ruel, MD MPH
Organizational Affiliation
Ottawa Heart Institute Research Corporation
Official's Role
Principal Investigator
Facility Information:
Facility Name
Lynn Heart and Vascular Institute, Boca Raton Regional Hospital
City
Boca Raton
State/Province
Florida
ZIP/Postal Code
33486
Country
United States
Facility Name
University of Ottawa Heart Institute
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1Y 4W7
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
21958773
Citation
Kulik A, Voisine P, Mathieu P, Masters RG, Mesana TG, Le May MR, Ruel M. Statin therapy and saphenous vein graft disease after coronary bypass surgery: analysis from the CASCADE randomized trial. Ann Thorac Surg. 2011 Oct;92(4):1284-90; discussion 1290-1. doi: 10.1016/j.athoracsur.2011.04.107.
Results Reference
background
PubMed Identifier
21934497
Citation
Kulik A, Ruel M. Lipid-lowering therapy and coronary artery bypass graft surgery: what are the benefits? Curr Opin Cardiol. 2011 Nov;26(6):508-17. doi: 10.1097/HCO.0b013e32834b9fb1.
Results Reference
background
PubMed Identifier
19673591
Citation
Kulik A, Ruel M. Statins and coronary artery bypass graft surgery: preoperative and postoperative efficacy and safety. Expert Opin Drug Saf. 2009 Sep;8(5):559-71. doi: 10.1517/14740330903188413.
Results Reference
background
PubMed Identifier
28611006
Citation
Kulik A, Abreu AM, Boronat V, Ruel M. Intensive versus moderate atorvastatin therapy and one-year graft patency after CABG: Rationale and design of the ACTIVE (Aggressive Cholesterol Therapy to Inhibit Vein Graft Events) randomized controlled trial (NCT01528709). Contemp Clin Trials. 2017 Aug;59:98-104. doi: 10.1016/j.cct.2017.06.006. Epub 2017 Jun 10.
Results Reference
derived

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Aggressive Cholesterol Therapy to Inhibit Vein Graft Events After CABG (ACTIVE Trial)

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