The objective of the present study is to determine the relation between vascular injury
induced by the stent and strut thickness.
Device: Polymer-free stent
Device: Biodegradable-polymer stent
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Full eligibility criteria for NCT03026465
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Patients older than 18 years
Ischemic symptoms or evidence of myocardial ischemia (inducible or spontaneous) in the presence of >50% de novo stenosis located in native coronary vessels
Target lesion located in the left main stem
Malignancies or other comorbid conditions with life expectancy less than 12 months or that may result in protocol noncompliance
Known allergy to the study medications (probucol, sirolimus, zotarolimus)
Pregnancy (present, suspected, or planned)
All locations for NCT03026465
Complejo Hospitalario Universitario de Vigo
Vigo, Pontevedra, Spain
Hospital Clinico San Carlos
Madrid, Spain, 28040
Hospital Universitario de La Princesa
View full eligibility
Tris trial is registered with FDA with number: NCT03026465. The sponsor of the trial is Fundacion Investigacion Interhospitalaria Cardiovascular and it is looking for 50 volunteers for the current phase.
Official trial title: Vessel Injury in Relation With Strut Thickness Assessed by OCT (VISTA): A Comparison of Vascular Injury Induced by a Polymer Free Sirolimus and Probucol Eluting Stent and a Biodegradable-polymer Biolimus-eluting Stent
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