CTOs are common among patients with angina, and are detected in around 20% of patients undergoing coronary angiography. Treatment of CTO has been found to constitute only 7% of PCI practice on average. One of the reasons for the under-presentation of CTOs in PCI target lesions is the lack of evidence-based medical data on treatment indications, and the continued low level of accepted evidence for the treatment of CTOs by PCI in PCI guidelines. Patients with a CTO represent patients with stable coronary artery disease. The COURAGE trial comparing PCI with optimal medical therapy in stable coronary disease did not show a difference in mortality or myocardial infarction between the two treatment options. However, CTOs were not included in the COURAGE trial. But that trial did confirm the superiority of PCI over OMT in controlling symptoms of angina, with a high cross-over rate to PCI. Whether PCI for CTO is superior to OMT in reducing MACE in those patients with a large ischaemic burden has never been tested in a randomized controlled trial. While there is compelling evidence from registry studies of a clinical and prognostic benefit following successful PCI of CTO compared with PCI failure, there has been no randomized controlled trial of contemporary PCI using drug-eluting stents versus optimal medical therapy. The COURAGE trial nuclear sub-study confirms both that prognosis is closely related to the extent of residual ischaemia and that PCI is more effective in reducing residual ischaemia than optimal medical therapy alone. This confirms earlier retrospective data suggesting that the benefit of PCI is greatest in patients with moderate (10-20%) or severe (\>20%) ischaemia. Study hypothesis: PCI with Biolimus eluting stent implantation plus OMT will be superior to OMT alone in improving health status at 12-month follow-up, and will be noninferior with respect to the composite of all cause death/ non fatal MI at 36-month follow up, in patients with a CTO in an epicardial coronary artery \>2.5 mm diameter and chronic stable angina with evidence of ischemia and viability in the territory subtended by the CTO
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
450
Recanalization of chronic coronary artery occlusion and subsequent implantation of one or ore Biosensor stents
Clinique Saint-Augustin
Bordeaux, France
CH de Lagny
Lagny, France
Institut Hospitalier Jacques Cartier - ICPS
Massy, France
Clinique Pasteur
Toulouse, France
Rangueil university hospital
Toulouse, France
Zentralklinik Bad Berka
Bad Berka, Germany
Herz-Zentrum Bad Krozingen
Bad Krozingen, Germany
Main Taunus Kliniken
Bad Soden, Germany
Klinikum Darmstadt
Darmstadt, Germany
Cardiac Catheterization Laboratory and Cardiovascular Interventional Unit Cannizzaro Hospita
Catania, Italy
...and 9 more locations
Quality of Life Seattle Angina Questionnaire (SAQ)
Seattle Angina Questionnaire and EQ-5D for health outcomes measurement
Time frame: Baseline and 12 months
Major cardiovascular events
Cumulative composite endpoint of cardiovascular death, non-fatal MI at 3 years
Time frame: 36 months
Safety and efficacy endpoints
All cause mortality Cardiac mortality Myocardial Infarction Any hospitalization due to cardiovascular events (angina, congestive heart failure, arrythmias) Repeat revascularization
Time frame: 12 and 36 months
Procedural complications
Incl. periprocedural enzyme leak (defined by CK increase \>3 times ULN); pericprocedural MI (new Q-wave or STEMI); pericardial tamponade, need for urgent CABG, CIN, death within 30 days, proven periprocedural cerebrovascular events
Time frame: baseline upto 36 months
Protocol adherence
Need to cross from OMT to PCI in Group 2 (after escalation up to maximum tolerated anti-anginal therapy and persistent unequivocal symptoms)
Time frame: 36 months
Per protocol analysis
primary endpoint comparison in patients who did have a successful revascularization compared to those patients treated medically who had no subsequent PCI
Time frame: 36 months
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