Revascularization Strategies in Patients With Non-ST-Segment Elevation Acute Coronary Syndrome (NSTE-ACS) and Severe Coronary Artery Disease
NCT ID: NCT01311323
Last Updated: 2025-09-25
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
1000 participants
INTERVENTIONAL
2025-08-25
2030-11-30
Brief Summary
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Similarly, all randomized studies comparing PCI vs CABG in multivessel disease included mainly patients with stable angina, small cohort of patients with unstable angina and they excluded patients with non ST elevation Myocardial infarction.
In the SYNTAX study -largest PCI vs CABG trial, randomized patients were patients with low perioperative risk (logistic EUROSCORE \<5) and ACS patients routinely excluded. High perioperative risk patients were included only in PCI registry.
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Detailed Description
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Aim and hypothesis:
Hence, the purpose of this study will be to compare contemporary coronary angioplasty with coronary artery bypass grafting in a prospective, clinical, multicenter, randomized trial. The hypothesis of this study is the non-inferiority of PCI compared to CABG in terms of the primary composite endpoint (death, myocardial infarction, stroke).
Method:
Patients with multivessel coronary artery disease, left main and acute coronary syndrome without ST segment elevation, qualified for early invasive treatment, with a Syntax Score below 33, and in whom the invasive cardiologist and cardiac surgeon will recognize both PCI and CABG as possible to achieve complete revascularization will be enrolled to the study. In the case of centers without the Cardiac Surgery Department, "Heart Team" consultations will take place via videoconference, and records of coronarography and echocardiography will be shared via the PACS (ang. Picture Archiving and Communication System system). The main exclusion criteria will be the qualification for conservative treatment, surgery other than CABG due to structural heart defect, ST segment elevation myocardial infarction, stable coronary artery disease, immediate need for PCI. After fulfilling the inclusion criteria and lack of exclusion criteria, the patient will be randomized in a 1: 1 ratio to either PCI or CABG. The PCI procedure will be performed after assessing the hemodynamic significance of all lesions with vFFR, FFR or iFR or using the latest generation drug eluting stents, and the implantation will be optimized based on intravascular imaging. CABG procedures will be performed based on the experience of the respective center, including the OPCAB technique, and the internal mammary artery will be used in each case. The primary endpoint of the study will be all cause death, myocardial infarction, and stroke in one-year follow-up. To prove the assumed hypothesis of the study, with the test power of 80% alpha error 5% and the percentage of lost to follow-up at the level of 5%, the study should include 500 patients in each group. Secondary endpoints will be ischemia driven revascularization, left ventricular ejection fraction, major and minor bleeding incidence, new onset of atrial fibrillation, de novo heart failure, unscheduled re-hospitalization, quality of life, and cost effectiveness. After the hospitalization, patients will be subjected to strict secondary prevention principles, including cardiac and cardiac surgery rehabilitation, and will undergo four specialistic follow-up visits with cardiac echo and stress tests at selected time points.
Anticipated outcomes:
In the case of positive results of the study, the efficacy and safety of PCI in the studied group of patients will be confirmed. This will contribute to the creation of a new guidelines in a given area, translating into faster and easier access to rapid invasive treatment. It will also facilitate the decision-making process in centers without cardiac surgery.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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PCI with DES implantation
Percutaneous Coronary Intervention Implantation of Drug-Eluting Stents
PCI
Percutaneous Coronary Intervention with contemporary drug eluting stent, fractional flow reserve or iFR measurement and optimisation with intravascular imaging
CABG
Coronary Artery Bypass Grafting.On-pump or Off-pump CABG
CABG
Coronary Artery Bypass Graft
Interventions
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PCI
Percutaneous Coronary Intervention with contemporary drug eluting stent, fractional flow reserve or iFR measurement and optimisation with intravascular imaging
CABG
Coronary Artery Bypass Graft
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Written patient consent,
* Acute Coronary Syndrome without ST-segment elevation of very high, high, and intermediate risk including NSTEMI and unstable angina requiring urgent (within 72 hours) invasive strategy,
* Qualification for invasive treatment,
* Multivessel coronary disease, defined as angiographic narrowing \>50%DS in at least two arteries, including involvement of the proximal segment of the left anterior descending artery or three-vessel disease with a Syntax Score \< 33. For borderline stenoses (40-70%), vFFR, FFR, or iFR will be decisive,
* Left main coronary artery disease defined as narrowing \>50%DS. For borderline changes, IVUS (MLA \<6 mm2 or vFFR, FFR, or iFR) with a Syntax Score \< 32 will be decisive,
* Feasibility of complete revascularization on both the CABG and PCI sides,
* Consent within the Heart Team for both CABG by the cardiothoracic surgeon and PCI by the interventional cardiologist.
Exclusion Criteria
* ST-segment elevation myocardial infarction (STEMI) or new left bundle branch block (LBBB),
* Stable coronary syndrome,
* Single- or two-vessel coronary disease without involvement of the proximal LAD, defined as narrowing above 50%DS,
* Qualification for conservative treatment,
* Anticipated surgery other than CABG due to severe valvular defect or other structural defect, particularly moderate or severe mitral regurgitation,
* Need for immediate coronary angioplasty treatment,
* Syntax Score above 33,
* Contraindications to short-term and long-term antiplatelet therapy,
* Acute heart failure in class IV (cardiogenic shock),
* Previous CABG procedure,
* Previous PCI procedure within the last 6 months,
* Ischemic or hemorrhagic stroke within 6 months prior to inclusion,
* End-stage chronic kidney disease on dialysis,
* Pregnancy or intention to become pregnant (women of child bearing age must have a recent negative pregnancy test prior to randomization),
* Non cardiac co-morbidities with life expectancy less than 3 years,
* Participation in other clinical trial that have not reached their primary endpoint.
18 Years
ALL
No
Sponsors
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Andrzej Frycz Modrzewski Krakow University
OTHER
American Heart of Poland
OTHER
Responsible Party
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Piotr P Buszman, MD
M.D., PhD, Professor
Principal Investigators
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Piotr P Buszman, MD,PhD, Prof
Role: PRINCIPAL_INVESTIGATOR
American Heart of Poland
Krzysztof Sanetra, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
American Heart of Poland
Locations
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Małopolska Cardiovascular Center, Polish-American Heart Clinic in Chrzanów
Chrzanów, Malopolska, Poland
Polish-American Heart Clinics Center for Cardiology and Cardiac Surgery Outpatient Specialist Care in Bielsko-Biała
Bielsko-Biala, Silesian Voivodeship, Poland
Polish-American Heart Clinics III Department of Invasive Cardiology, Angiology and Electrocardiology
Dąbrowa Górnicza, Silesian Voivodeship, Poland
Polish-American Heart Clinics, 1st Department of Cardiology and Angiology in Ustroń
Ustroń, Silesian Voivodeship, Poland
Polish-American Heart Clinics X Department of Invasive Cardiology, Electrophysiology and Electrostimulation in Tychy
Tychy, , Poland
Countries
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Central Contacts
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Facility Contacts
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References
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Park DW, Kim YH, Yun SC, Lee JY, Kim WJ, Kang SJ, Lee SW, Lee CW, Kim JJ, Choo SJ, Chung CH, Lee JW, Park SW, Park SJ. Long-term outcomes after stenting versus coronary artery bypass grafting for unprotected left main coronary artery disease: 10-year results of bare-metal stents and 5-year results of drug-eluting stents from the ASAN-MAIN (ASAN Medical Center-Left MAIN Revascularization) Registry. J Am Coll Cardiol. 2010 Oct 19;56(17):1366-75. doi: 10.1016/j.jacc.2010.03.097.
Park DW, Seung KB, Kim YH, Lee JY, Kim WJ, Kang SJ, Lee SW, Lee CW, Park SW, Yun SC, Gwon HC, Jeong MH, Jang YS, Kim HS, Kim PJ, Seong IW, Park HS, Ahn T, Chae IH, Tahk SJ, Chung WS, Park SJ. Long-term safety and efficacy of stenting versus coronary artery bypass grafting for unprotected left main coronary artery disease: 5-year results from the MAIN-COMPARE (Revascularization for Unprotected Left Main Coronary Artery Stenosis: Comparison of Percutaneous Coronary Angioplasty Versus Surgical Revascularization) registry. J Am Coll Cardiol. 2010 Jul 6;56(2):117-24. doi: 10.1016/j.jacc.2010.04.004. Epub 2010 May 6.
Buszman PE, Buszman PP, Kiesz RS, Bochenek A, Trela B, Konkolewska M, Wallace-Bradley D, Wilczynski M, Banasiewicz-Szkrobka I, Peszek-Przybyla E, Krol M, Kondys M, Milewski K, Wiernek S, Debinski M, Zurakowski A, Martin JL, Tendera M. Early and long-term results of unprotected left main coronary artery stenting: the LE MANS (Left Main Coronary Artery Stenting) registry. J Am Coll Cardiol. 2009 Oct 13;54(16):1500-11. doi: 10.1016/j.jacc.2009.07.007. Epub 2009 Aug 21.
Buszman PP, Bochenek A, Konkolewska M, Trela B, Kiesz RS, Wilczynski M, Cisowski M, Krejca M, Banasiewicz-Szkrobka I, Krol M, Kondys M, Wiernek S, Orlik B, Martin JL, Tendera M, Buszman PE. Early and long-term outcomes after surgical and percutaneous myocardial revascularization in patients with non-ST-elevation acute coronary syndromes and unprotected left main disease. J Invasive Cardiol. 2009 Nov;21(11):564-9.
Buszman PE, Kiesz SR, Bochenek A, Peszek-Przybyla E, Szkrobka I, Debinski M, Bialkowska B, Dudek D, Gruszka A, Zurakowski A, Milewski K, Wilczynski M, Rzeszutko L, Buszman P, Szymszal J, Martin JL, Tendera M. Acute and late outcomes of unprotected left main stenting in comparison with surgical revascularization. J Am Coll Cardiol. 2008 Feb 5;51(5):538-45. doi: 10.1016/j.jacc.2007.09.054.
Other Identifiers
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AHP-1
Identifier Type: -
Identifier Source: org_study_id
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