Coronary Heart Disease
Conditions
Brief summary
This prospective, randomized trial will compare the extent of covered stent strut segments by assessed by Optical Coherence Tomography (OCT) of the ORSIRO DES with that of the XIENCE PRIME DES, which is the standard of choice of contemporary drug eluting stents (DES).
Detailed description
The ORSIRO drug eluting stent exhibits a favourable vascular healing profile from baseline to 6 months assessed by optical coherence tomography (OCT). Patients with symptomatic coronary artery disease without cardiogenic shock who will undergo coronary angiography and willing to participate in the trial will receive before the procedure a loading dose of P2Y12 antagonists (clopidogrel, prasugrel or ticagrelor). Eligible patients who do not meet the exclusion criteria and for whom PCI will be considered as the appropriate form of revascularization will be randomly assigned to the ORSIRO or the XIENCE PRIME DES in the relation 1 x ORSIRO: 1 x XIENCE PRIME. All patients will receive periprocedural intravenous aspirin and heparin or bivalirudin. After the intervention patients will receive aspirin indefinitely and P2Y12 antagonists for at least 6 months. The intravascular imaging by OCT will be performed at the 6-8 months follow-up angiography.
Interventions
DEVICEXIENCE PRIME DES
due randomization XIENCE PRIME DES will be implanted
DRUGORSIRO
due randomization ORSIRO will be implanted
Sponsors
Technical University of Munich
Deutsches Herzzentrum Muenchen
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Patients older than age 18 with ischemic symptoms or evidence of myocardial ischemia in the presence of ≥ 50% stenosis located in native coronary vessels. * Written, informed consent by the patient or her/his legally-authorized representative for participation in the study. * In women with childbearing potential a negative pregnancy test is mandatory. * AHA type A, B1 and B2 lesions.
Exclusion criteria
* Lesion length \> 25 mm requiring a stent length \> 28 mm * Target lesion located in the left main trunk. * In-stent restenosis. * Acute myocardial infarction * Malignancies or other comorbid conditions (for example severe liver, renal and pancreatic disease) with life expectancy less than 18 months or that may result in protocol non-compliance. * Known allergy to the study medications: sirolimus, everolimus * Inability to take dual antiplatelet therapy for at least 6 months. * The presence of bifurcation lesions * The presence of calcified lesions * Pregnancy (present, suspected or planned) or positive pregnancy test. * Previous enrollment in this trial. * Patient's inability to fully cooperate with the study protocol
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Degree of stent strut coverage at 6 months follow-up assessed by OCT for each visible strut segment | 6-18 months |
Countries
Germany
Outcome results
None listed