Drug-eluting-stents for Unprotected Left Main Stem Disease (ISAR-LEFT-MAIN)
Coronary Disease

About this trial
This is an interventional treatment trial for Coronary Disease
Eligibility Criteria
Inclusion Criteria: Patients older than age 18 with ischemic symptoms or evidence of myocardial ischemia in the presence of ≥50% stenosis located in unprotected LMCA who are unable to undergo coronary artery bypass graft (CABG) Pretreatment with a loading dose of 300-600 mg clopidogrel Informed, written consent Exclusion Criteria: Cardiogenic shock; ST-segment elevation acute myocardial infarction within 48 h from symptom onset; In-stent restenosis; Malignancies or other comorbid conditions with life expectancy less than one year; Prior coronary artery bypass surgery with revascularization of left anterior descending (LAD) and/or left circumflex (LCx) coronary artery Planned staged percutaneous coronary intervention (PCI) procedure within 30 days from index procedure or prior PCI within the last 30 days Left main size >4.5mm An elective surgical procedure is planned during the first six months post enrolment; Known allergy to the study medications Pregnancy Patient's inability to fully cooperate with the study protocol
Sites / Locations
- Deutsches Herzzentrum
- First Medizinische Klinik, Klinikum rechts der Isar
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
A
B
Sirolimus-eluting stent (Cypher)
Paclitaxel-eluting stent (Taxus)