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
- 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
- Severe tortuosity
- Severe calcification
All locations for NCT03027856
Aarhus N, Denmark, 8000
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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