Study of the Orsiro Drug Eluting Stent System
- Conditions
- Coronary Artery Disease
- Registration Number
- NCT01356888
- Lead Sponsor
- Biotronik AG
- Brief Summary
The purpose of this study is to compare the BIOTRONIK Orsiro Drug Eluting Stent System with the Abbott Xience Prime™ Drug Eluting Stent System with respect to in-stent Late Lumen Loss in a non-inferiority study in de novo coronary lesions at 9 months.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 452
- Subject has provided a written informed consent
- Single de novo lesion with ≥ 50% and <100% stenosis in up to 2 coronary arteries
- The target lesion length is ≤ 26 mm
- The target reference vessel diameter is ≥ 2.25 mm and ≤ 4.0 mm
Main
- Evidence of myocardial infarction within 72 hours prior to index procedure
- Unprotected left main coronary artery disease (stenosis >50%)
- Three-vessel coronary artery disease at time of procedure Thrombus in target vessel
- Target lesion involves a side branch > 2.0 mm in diameter
- Heavily calcified lesion
- Target lesion is located in or supplied by an arterial or venous bypass graft
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Late Lumen Loss 9 months post index procedure
- Secondary Outcome Measures
Name Time Method
Related Research Topics
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Trial Locations
- Locations (24)
Klinikum Wels-Grieskirchen
🇦🇹Wels, Oberoesterreich, Austria
Hospital Prive Jacques Cartier Massy
🇫🇷Massy, France
CHU - Hospital Arnaud de Villeneuve
🇫🇷Montpellier, France
Polyclinique les Fleurs Ollioules
🇫🇷Ollioules, France
Heart Centre Bad Krozingen
🇩🇪Bad Krozingen, Germany
Heart- and Diabetescentre NRW
🇩🇪Bad Oeyenhausen, Germany
Segeberger Kliniken GmbH
🇩🇪Bad Segeberg, Germany
Charité Campus Mitte
🇩🇪Berlin, Germany
Charité Campus Benjamin Franklin
🇩🇪Berlin, Germany
Universityhospital Lübeck
🇩🇪Lübeck, Germany
Scroll for more (14 remaining)Klinikum Wels-Grieskirchen🇦🇹Wels, Oberoesterreich, Austria