Coronary Artery Bypass Surgery (CABG) Off or On Pump Revascularization Study (CORONARY)
I. Main Research Question:
- To compare the risks and benefits of Off-pump Coronary artery bypass surgery (CABG) to On-pump CABG and to determine if one is better than the other.
- The purpose of this pilot study is also to see the rate of recruitment with expertise-based randomization across different hospital settings.
II. Small RCT studies and meta-analyses done so far have not been able to conclusively say which of the procedure is better. A large randomized study is required to establish the risks and benefits associated with both the off-pump and on-pump CABG surgical procedures.
III. The study will look at which of the two techniques reduce major risks associated with CABG.
|the Efficacy and Safety of Off-pump CABG||Procedure: Coronary Artery Bypass Graft with the use of CPB Procedure: Coronary Artery Bypass Graft without the use of CPB||Phase 3|
|Study Design:||Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
|Official Title:||CABG Off or On Pump Revascularization Study (CORONARY)|
- First Co-Primary Outcome [ Time Frame: 30 days post CABG surgery ]The occurrence of the composite of total mortality, stroke, nonfatal MI, or new renal failure at 30 days post CABG surgery
- Second co-primary outcome [ Time Frame: 5 years after CABG ]The occurrence of the composite of total mortality, stroke, nonfatal MI, new renal failure, or repeat coronary revascularization (i.e. coronary artery bypass surgery or percutaneous coronary intervention) over 5 years after randomization.
- The assessment of total costs and resources consumption at 30 days after CABG surgery [ Time Frame: 30 days after CABG surgery ]
- The assessment of total costs and resources consumption at 5 years after CABG surgery [ Time Frame: 5 years after CABG surgery ]
|Study Start Date:||October 2007|
|Study Completion Date:||September 2016|
|Primary Completion Date:||March 2012 (Final data collection date for primary outcome measure)|
|Active Comparator: On Pump Arm||
Procedure: Coronary Artery Bypass Graft with the use of CPB
Coronary Artery Bypass Graft (CABG) using median sternotomy, CPB, cardioplegia and complete cross-clamp and no associated or concomitant surgical procedures
Other Name: ON Pump CABG
|Experimental: Off Pump Arm||
Procedure: Coronary Artery Bypass Graft without the use of CPB
Coronary Artery Bypass Graft (CABG) with no associated or concomitant surgical procedures, using median sternotomy and without CPB and cardioplegia
Other Name: OFF Pump
Hide Detailed Description
Rationale and purpose of the study:
Coronary artery bypass grafting (CABG) surgery prolongs life-expectancy in patients with severe ischemic heart disease, especially those with left main, triple vessel disease or single/double vessel disease with stenosis of the proximal left anterior descending (LAD) artery. The perioperative mortality is about 2% with an additional 5% to 7% suffering complications such as myocardial infarction, stroke, renal failure, etc. The technique of operating on a beating heart (off-pump) for coronary artery bypass grafting surgery has been recently developed in the past few years in an effort to decrease the above perioperative complications typically related to cardiopulmonary bypass associated with on-pump CABG. While registries suggest that off-pump CABG may be superior, these data cannot fully control for differences in patient characteristics, which influence patient selection for specific procedures. The benefits of off-pump CABG compared with conventional on-pump CABG are unclear. The investigators therefore propose a large simple, international multicentre randomized controlled trial to definitively evaluate the efficacy and safety of off-pump CABG in the treatment of patients undergoing coronary artery surgery funded by CIHR, this pilot study will be a preliminary step towards a full trial.
The investigators examined the outcomes in the Canadian off-pump CABG Registry to identify a group of patients who represent a higher risk of cardiovascular events. Utilizing the inclusion criteria described below, this group of patients has accumulated the vast majority of outcomes in the Registry and represent more than 50% of patients in the Registry, therefore minimizing the sample size but still being representative. The cumulative event rate at 30 days (first co-primary outcome) for on-pump CABG is estimated as being 8.6% and the investigators expect a 33% relative risk reduction (RRR) for the off-pump CABG group. The sample calculated for the whole trial is 4700 patients.
Trial design: This is a pilot randomized controlled trial comparing off-pump CABG versus on-pump CABG in 60 patients who will be undergoing isolated CABG.
Interventions: Patients eligible for CABG will be randomized to receive either an Off-pump CABG surgery or On-pump CABG surgery.
Randomization: After obtaining informed written consent patients will be allocated to either off-pump CABG or on-pump CABG by calling a 24-hour randomization telephone number. An expertise-based randomization will be used wherein a surgeon who is an expert in Off-pump surgery will operate on patients randomized to receive Off-pump surgery. Patients randomized to receive On-pump CABG will be operated on by a surgeon who is an expert in on-pump CABG surgery. To minimize bias stratified block randomization will used. For this pilot study randomization will be stratified to 3 centres and random block of 4 or 6.
The data adjudicators will be blinded to the study. Due to the nature of intervention, the operating surgeon, anesthetist, perfusionist, other operation room staff, intensive-care unit staff will not be blinded in this study.
Patients will have either been seen in the emergency, outpatient or ICU and diagnosed with having single, double or triple coronary artery occlusion requiring an isolated CABG.
Interventions: Patients eligible for CABG will be randomized to receive either an Off-pump CABG surgery or On-pump CABG surgery. A surgeon who is an expert in the assigned technique will perform the procedure.
- The occurrence of the composite of total mortality, stroke, nonfatal MI, or new renal failure at 30 days post CABG surgery AND
- The occurrence of the composite of total mortality, stroke, nonfatal MI, new renal failure, or repeat coronary revascularization (i.e. coronary artery bypass surgery or percutaneous coronary intervention) over 5 years after randomization.
The secondary outcomes
- The assessment of total costs and resources consumption at 30 days after CABG surgery AND
- The assessment of total costs and resources consumption at 5 years after CABG surgery
The investigators will ascertain all events of interest through periodic and regular follow-up utilizing standardized definitions for all events, appropriate supporting documents will be obtained centrally.
- CV death: all deaths are considered cardiovascular unless a specific non-cardiovascular cause is evident (e.g. malignancy).
- Stroke: new acute focal neurological deficit (except for subarachnoid hemorrhage which may not be focal) thought to be of vascular origin with signs or symptoms lasting greater than 24 hours.
- MI perioperative (within 24 hours of surgery): new pathologic Q waves with documented new wall motion abnormalities other than septal OR cardiac markers ³ 10 x ULN.
- MI non-perioperative (later than 24 hours after surgery): ECG changes consistent with infarction (new significant Q waves in two contiguous leads in the absence of previous LVH or conduction abnormalities) or evolving ST-segment to T-wave changes in two contiguous leads or new left bundle branch block or ST segment elevation requiring thrombolysis or PCI AND cardiac markers (troponins or CKMB) in the necrosis range. Post-PCI MI are included into non-perioperative MI group but are defined as new pathologic Q waves with documented new wall motion abnormalities other than septal OR cardiac markers ³ 3 x ULN within 24 hours of PCI.
- Renal failure: doubling of serum creatinine from pre-op baseline or requirement for renal replacement therapy (eg, dialysis, continuous hemofiltration, renal transplant). Hemofiltration or dialysis only during cardio-pulmonary bypass does not constitute a requirement for renal replacement therapy. Patients who receive dialysis within 1 month of the surgery are not eligible for this endpoint.
- Repeated coronary revascularization: new CABG procedure or PCI associated with documented ischemia by stress testing (ECG, ECHO, or nuclear) AND graft failure or new culprit lesion (³ 70% luminal stenosis).
For other endpoints, the investigators have defined:
- Recurrence of angina: new or chronic onset of typical chest pain with documented ischemia by stress testing (ECG, ECHO, or nuclear).
- Blood transfusions: all blood bank products transfused within 24 hours of the CABG surgery.
- Total mortality: all causes of mortality
Plan for data analysis:
The intention to treat principle, in which all participants will be included in their assigned treatment groups regardless of adherence, will guide all analyses. In the principle analysis, the time to the first occurrence of one of the components of the cluster of (cardiac death, stroke, nonfatal MI, new renal failure) will be presented by Kaplan-Meier survival curves and the comparisons between the two treatment groups will be performed by a log-rank test. The treatment effect as measured by the hazard ratio and 95% confidence interval will be derived by the Cox proportional hazards model. The investigators will also calculate the absolute risk reductions and the associated 95% confidence intervals, as well as the number needed to treat (NNT) with off-pump CABG to prevent one major cardiovascular event. Participants who prematurely discontinue follow-up before a major cardiovascular event will be censored as to their last follow-up data; this number is expected to be <1% given the relatively short period of follow-up after surgery.
In secondary analyses the investigators will determine and compare the incidence of major cardiovascular events (cardiac death, stroke, nonfatal MI, new renal dialysis) and revascularization procedures (i.e. coronary artery bypass surgery and percutaneous coronary intervention) using the same strategy. The effect of the two operative techniques on different sub-groups (i.e. patients with diabetes, renal failure, congestive heart failure, cerebrovascular disease, as well as patient left ventricular function, gender and ages will be conducted by stratified analysis through a Cox proportional hazards model. The test of interaction between each subgroup factor and the treatment group will be done by including a product term in the model already containing treatment and the subgroup factor. The length of hospital stay and length of ICU/CCU stay will be compared using a student's t-test. An events adjudication committee (blind to surgical allocation) will centrally review all suspected major outcomes listed above.
The investigators will also do subgroup analysis on different sub-groups (i.e. patients with diabetes, renal failure, congestive heart failure, cerebrovascular disease, as well as patient left ventricular function, gender and ages will be examined for consistency and coherence)
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00463294
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00463294
Hide Study Locations
|Fundacion Medica de rio negro y neuquen|
|Rio Negro, Argentina|
|Beneficencia Portuguesa de Sao Paulo|
|Sao Paulo,, CEP, Brazil, 01323.001|
|Instituto Dante Pazzanese de Cardiologia|
|Sao Paulo, CEP, Brazil, 04012-909|
|Hospital Sao Francisco Complexo Hospitalar Santa Casa|
|Porto Alegre, RS, Brazil, 90020-090|
|Irmande Santa Casa De Misericordia De Curtiba|
|Curitiba Parana, Brazil, 80010030|
|Braile Clinica de Servicos de Assistencia Medico|
|Sao Jose do Rio Preto, Brazil, 15091-450|
|Irmandade da Santa Casa de Misericordia de Sao Paulo|
|Sao Paulo, Brazil, 01221-020|
|Federal University of Sao Paulo School of Medicine|
|Sao Paulo, Brazil, 04024-002|
|Instituto do Coracao do Hospital das Clinicas da|
|Sao Paulo, Brazil, 05403-00|
|Hospital Mario Covas|
|Sao Paulo, Brazil, 09190-615|
|Santa Casa de Misericordia de Marilia|
|Sao Paulo, Brazil, 17515-000|
|Associação do Sanátorio Sírio|
|São Paulo, Brazil, 04038-030|
|Foothills Medical Centre|
|Calgary, Alberta, Canada, T2N 2T9|
|Hamilton General Hospital|
|Hamilton, Ontario, Canada, L8L 2X2|
|London Health Sciences Centre|
|London, Ontario, Canada, N6A 5A5|
|Toronto General Hospital|
|Toronto, Ontario, Canada, M5G 2C4|
|Montreal Heart Institute|
|Montreal, Quebec, Canada, H1T 1C8|
|Hotel-Dieu du CHUM|
|Montreal, Quebec, Canada, H2W 1T8|
|Hospital Regional Temuco|
|Temuco, IX Region, Chile|
|Instituto Nacional del Torax|
|Nanjing First Hospital|
|Fundacion Valle Del Lili|
|Charles University Hospital|
|Hradec Kralove, Czech Republic, 50005|
|Ostrava-Poruba, Czech Republic, 708 52|
|University Hospital Pilsen|
|Pilsen, Czech Republic, 304 60|
|Fakultni nemocnice Kralovske Vinohrady (FNKV)|
|Prague, Czech Republic, 100 34|
|University Hospital Motol|
|Praha, Czech Republic, 150 00|
|Trinec, Czech Republic, 739 61|
|Service de chirurgie thoracique et cardio-vasculaire|
|Besancon, France, 25030|
|Nizam's Institute of Medical Sciences|
|Hyderabad, Andhra Pradesh, India, 500 082|
|SAL Hospital and Medical Institute|
|Ahmedabad, Gujarat, India, 380054|
|Amrita Institute of Medical Sciences and Research Center|
|Cochin, Kerala, India, 682 026|
|G.Kuppuswamy Naidu Memorial Hospital|
|Coimbatore, TamilNadu, India, 641 037|
|International Center of Cardiovascular and Thoracic Diseases|
|Chennai Tamil Nadu, India, 600101|
|Sanjay Gandhi PGIMS|
|Lucknow, India, 226 014|
|All India Institute of Medical Sciences|
|New Delhi, India, 110016|
|Escorts Heart Institute and Research Centre|
|Noida, India, 201307|
|Ospedale S. Croce|
|Cuneo, Italy, 12100|
|Ospedale Niguarda - Ca Granda|
|Milano, Italy, 20162|
|Krakow, Poland, 31-202|
|Sertap Aykut Aka|
|Basildon and Thurrock University Hospital NHS FT|
|Basildon, Essex, United Kingdom, SS16 5NL|
|Royal Infirmary of Edinburgh|
|Edinburgh, EU, United Kingdom, 16 4SU|
|The John Radcliffe Hospital|
|Oxford, United Kingdom, OX3 9DU|
|Principal Investigator:||Lamy Andre, MD, MSc||McMaster University|
|Principal Investigator:||Salim Yusuf, MD, DPhil||Population Health Research Institute|
|Principal Investigator:||David Taggart, MD||University of Oxford|