Impact of High-dose Pretreatment of Rosuvastatin in Patients With Acute Coronary Syndrome Following Off-pump Coronary Artery Bypass: Results From the HIROP-ACS (HIgh-dose Pretreatment of Rosuvastatin During Off-Pump Coronary Bypass in Acute Coronary Syndrome) Study
Primary Purpose
A Total of 234 Patients With Acute Coronary Syndrome Who Will Undergo OPCAB.
Status
Completed
Phase
Phase 4
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Rosuvastatin
Sponsored by
About this trial
This is an interventional supportive care trial for A Total of 234 Patients With Acute Coronary Syndrome Who Will Undergo OPCAB. focused on measuring Statin, coronary artery bypass grafting, off-pump surgery, acute coronary syndrome
Eligibility Criteria
Inclusion Criteria:
- The presence of acute coronary syndrome, including unstable angina, acute non-ST elevation myocardial infarction
- Age of 19 years or older
- A need for isolated surgical myocardial revascularization
- Patients with signed informed consent
Exclusion Criteria:
- Patients with combined surgery with coronary bypass grafting
- On-pump conversion
- Patients with any increase in liver enzymes
- Patients with history of liver or muscle disease.
- Patients with moderate renal dysfunction (creatinine>2.0mg/dl) or need for dialysis
- Re-do surgery
- Urgent/emergent surgery
Sites / Locations
- Division of Cardiovascular Surgery, Severance Cardiovascular Hospital , Yonsei University College of Medicine
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Rosuvastatin group
Placebo group
Arm Description
Rosuvastatin group
Placebo group
Outcomes
Primary Outcome Measures
Major adverse cardiac events (MACEs)
Major adverse cardiac events (MACEs), which include the following: death from all causes, non-fatal myocardial infarction (MI), and repeat revascularization by percutaneous intervention or bypass surgery within 30 days after OPCAB.
Secondary Outcome Measures
The degree of myocardial ischemia and inflammatory
The degree of myocardial ischemia and inflammatory changes assessed by blood sampling and specific tests (CK-MB, Troponin T, ESR, CRP, hs-CRP) at the early period after OPCAB.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01971606
Brief Title
Impact of High-dose Pretreatment of Rosuvastatin in Patients With Acute Coronary Syndrome Following Off-pump Coronary Artery Bypass: Results From the HIROP-ACS (HIgh-dose Pretreatment of Rosuvastatin During Off-Pump Coronary Bypass in Acute Coronary Syndrome) Study
Study Type
Interventional
2. Study Status
Record Verification Date
October 2013
Overall Recruitment Status
Completed
Study Start Date
October 2007 (undefined)
Primary Completion Date
June 2012 (Actual)
Study Completion Date
March 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Yonsei University
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Periprocedural treatment with high-dose statins is known to have cardioprotective and pleiotropic effects, such as anti-thrombotic and anti-inflammatory actions.
-Objective: to determine whether preoperative rosuvastatin loading is independently associated with reduced myocardial ischemia and clinical outcomes in patients with stable angina undergoing isolated off-pump coronary bypass (OPCAB) in patients with acute coronary syndrome.
Study design
Prospective, double-blinded, single-center study of each 117 subjects enrolled
Subjects with acute coronary syndrome who meet all inclusion and exclusion criteria will be enrolled preoperatively.
Eligible subjects will be randomized 1:1 to A) High-dose rosuvastatin (n=117) vs. B) Placebo (n=117).
The amount of preoperative administration of high-dose rosuvastatin will be 60mg of a total
All subjects will undergo OPCAB procedure. - The primary and secondary endpoints will be compared at 30 days and 2 years postoperatively between two groups
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
A Total of 234 Patients With Acute Coronary Syndrome Who Will Undergo OPCAB.
Keywords
Statin, coronary artery bypass grafting, off-pump surgery, acute coronary syndrome
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
234 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Rosuvastatin group
Arm Type
Experimental
Arm Description
Rosuvastatin group
Arm Title
Placebo group
Arm Type
Placebo Comparator
Arm Description
Placebo group
Intervention Type
Drug
Intervention Name(s)
Rosuvastatin
Intervention Description
Patients will be randomized in a ratio of 1:1 to A) High-dose rosuvastatin vs. B) Placebo.
A) Rosuvastatin group : Administration of 40mg of rosuvastatin PO 12 hours before surgery and 20mg of rosuvastatin PO 2hours before surgery and 10mg of rosuvastatin PO daily at postoperative period.
B) Placebo group : Administration of placebo at 12 hours and 2 hours before surgery and 10mg of rosuvastatin PO daily at postoperative period.
Primary Outcome Measure Information:
Title
Major adverse cardiac events (MACEs)
Description
Major adverse cardiac events (MACEs), which include the following: death from all causes, non-fatal myocardial infarction (MI), and repeat revascularization by percutaneous intervention or bypass surgery within 30 days after OPCAB.
Time Frame
30 days after OPCAB
Secondary Outcome Measure Information:
Title
The degree of myocardial ischemia and inflammatory
Description
The degree of myocardial ischemia and inflammatory changes assessed by blood sampling and specific tests (CK-MB, Troponin T, ESR, CRP, hs-CRP) at the early period after OPCAB.
Time Frame
immediate, 24 hours, 48 hours, 72 hours, 7 days after OPCAB
Other Pre-specified Outcome Measures:
Title
Incidence of postoperative atrial arrhythmia including atrial fibrillation and atrial flutter
Time Frame
30 days after OPCAB
Title
Incidence of postoperative renal impairment or a need for dialysis
Time Frame
30 days after OPCAB
Title
Late MACEs 2 years after OPCAB
Time Frame
2 years after OPCAB
10. Eligibility
Sex
All
Minimum Age & Unit of Time
19 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
The presence of acute coronary syndrome, including unstable angina, acute non-ST elevation myocardial infarction
Age of 19 years or older
A need for isolated surgical myocardial revascularization
Patients with signed informed consent
Exclusion Criteria:
Patients with combined surgery with coronary bypass grafting
On-pump conversion
Patients with any increase in liver enzymes
Patients with history of liver or muscle disease.
Patients with moderate renal dysfunction (creatinine>2.0mg/dl) or need for dialysis
Re-do surgery
Urgent/emergent surgery
Facility Information:
Facility Name
Division of Cardiovascular Surgery, Severance Cardiovascular Hospital , Yonsei University College of Medicine
City
Seoul
ZIP/Postal Code
120-752
Country
Korea, Republic of
12. IPD Sharing Statement
Citations:
PubMed Identifier
17394957
Citation
Patti G, Pasceri V, Colonna G, Miglionico M, Fischetti D, Sardella G, Montinaro A, Di Sciascio G. Atorvastatin pretreatment improves outcomes in patients with acute coronary syndromes undergoing early percutaneous coronary intervention: results of the ARMYDA-ACS randomized trial. J Am Coll Cardiol. 2007 Mar 27;49(12):1272-8. doi: 10.1016/j.jacc.2007.02.025.
Results Reference
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Impact of High-dose Pretreatment of Rosuvastatin in Patients With Acute Coronary Syndrome Following Off-pump Coronary Artery Bypass: Results From the HIROP-ACS (HIgh-dose Pretreatment of Rosuvastatin During Off-Pump Coronary Bypass in Acute Coronary Syndrome) Study
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