The purpose of this study is to investigate the feasibility and safety of the Magmaris BRS
for treatment of coronary bifurcation lesions.
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Locations near you
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Full eligibility criteria for NCT03027856
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Stable angina pectoris
Stabilized non-ST elevation myocardial infarction
Silent angina pectoris
Age > 18 years
De novo coronary bifurcation lesion at LAD/diagonal, CX/obtuse marginal or RCA-PDA/posterolateral branch
All Medina classes except Medina x.x.1.
Diameter of side branch ≥ 2.5 mm
Side branch diameter stenosis less than 50%
Signed informed consent
ST-elevation infarction within 48 hours
Expected survival < 1 year
Severe heart failure (NYHA≥III)
S-creatinine > 120 µmol/L or GFR < 0.45 mL/min per 1.73 m2
Allergy to contrast media, aspirin, clopidogrel, ticagrelor, ticlopidine or sirolimus
Unable to cover main vessel lesion with one stent
All locations for NCT03027856
Aarhus University Hospital
Aarhus N, Denmark, 8000
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View full eligibility
Tris trial is registered with FDA with number: NCT03027856. The sponsor of the trial is Aarhus University Hospital Skejby and it is looking for 20 volunteers for the current phase.
Official trial title: A Sirolimus Eluting Bioresorbable Magnesium Stent for Treatment of Coronary Bifurcation Lesions - The BIFSORB Pilot Study II
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