This registry is a clinical post-market evaluation of the Orsiro LESS in subjects requiring
coronary revascularization with Drug Eluting Stents (DES).
We will connect you to the doctor responsible for this trial and help you get more information.
Locations near you
Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Full eligibility criteria for NCT01593059
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Symptomatic coronary artery disease
Subject has signed informed consent for data release
Subject is geographically stable and willing to participate at all follow-up assessments
Subject is ≥ 18 years
Elective PCI with DES
Subject did not sign informed consent for data release
Known intolerance to aspirin, clopidogrel, ticlopidine, heparin or any other anticoagulation / antiplatelet therapy required for PCI, stainless steel, Sirolimus or contrast media
Planned surgery within 6 months of PCI unless dual antiplatelet therapy will be maintained
Currently participating in another study and primary endpoint is not reached yet.
All locations for NCT01593059
Cardiovascular Diseases Institute CC Iliescu
University Hospital Bucharest
County Emergency Hospital
Cluj Napoca, Romania
Targu Mures, Romania, 540136
View full eligibility
Tris trial is registered with FDA with number: NCT01593059. The sponsor of the trial is Biotronik Vertriebs-GmbH and it is looking for 13 volunteers for the current phase.
Official trial title: BIOTRONIK - SaFety and Performance Registry for an All-comers Patient Population With the Limus Eluting Orsiro Stent System Within Daily Clinical Practice - III Romania
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