| Primary | Major Cardiac Adverse Events (Including Cardiac Death, Myocardial Infarction (Q-wave and Non Q-wave) and Clinically Driven TLR (Target Lesion Revascularization)) | Major adverse cardiac and cerebral events are defined as an adjudicated composite of cardiac death, myocardial infarction (Q-wave and non Q-wave), emergent coronary artery bypass surgery and target vessel revascularization (TVR). The primary safety measure was the composite of MACE up to 12 months follow up. In order to show the safety of the device, the MACE rate was compared with the performance goal for bare metal stents(experience with bare metal stents in clinical trials suggested that the 12 month MACE rate should be about 25.0%). | No formal statistical significance testing was performed. Descriptive statistics were calculated for all relevant variables (mean, standard deviation, median and ranges for the continuous variables and with frequencies and % for the discrete variables). Subjects who discontinued prematurely were included in the analysis and were not replaced. | Posted | | Number | | participants | | at 12 months follow-up | | | | ID | Title | Description |
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| OG000 | Treated With Presillion Stent | Patients treated with the Presillion stent in up to two de novo coronary artery lesions |
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| Secondary | Device Success | Device success defined as achievement of a final diameter stenosis of <50% (by visual estimate), using the assigned device only | 318 patients treated with the Presillion stent in up to two de novo coronary artery lesions (354 lesions) | Posted | | Number | | percentage of device success | | Peri-procedure up to discharge | Lesions | Participants | | ID | Title | Description |
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| OG000 | Treated With Presillion Stent | Patients treated with the Presillion stent in up to two de novo coronary artery lesions |
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| Secondary | Lesion Success | Lesion success defined as the attainment of <50% final diameter stenosis (by visual estimate) using any percutaneous method. | 318 patients treated with the Presillion stent in up to two de novo coronary artery lesions (354 lesions) | Posted | | Number | | percentage of lesion Success | | Peri-procedure up to discharge | Lesion | Participants | | ID | Title | Description |
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| OG000 | Treated With Presillion Stent | Patients treated with the Presillion stent in up to two de novo coronary artery lesions |
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| Secondary | Procedural Success | Procedural success defined as achievement of a final diameter stenosis of <50% (by visual estimate) using any percutaneous method, without the occurrence of death, MI (Myocardial Infarction), or repeat revascularization of the target lesion during the hospital stay | 318 patients treated with the Presillion stent in up to two de novo coronary artery lesions (354 lesions) | Posted | | Number | | percentage of Procedural Success | | Peri-procedure up to discharge | Lesions | Participants | | ID | Title | Description |
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| OG000 | Treated With Presillion Stent | Patients treated with the Presillion stent in up to two de novo coronary artery lesions |
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| Secondary | Clinically Driven TLR | Target Lesion Revascularization (TLR) is defined as any clinically-driven repeat percutaneous intervention of the target lesion or bypass surgery of the target vessel | 309 patients treated with the Presillion stent in up to two de novo coronary artery lesions (311 lesions) | Posted | | Number | | participants | | Up to 30 days | Lesions | Participants | | ID | Title | Description |
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| OG000 | Treated With Presillion Stent | Patients treated with the Presillion stent in up to two de novo coronary artery lesions |
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| Secondary | Clinically Driven TVR | Target vessel revascularization (TVR) is defined as any clinically driven (as defined for TLR) repeat percutaneous intervention of the target vessel or bypass surgery of the target vessel. | 309 patients treated with the Presillion stent in up to two de novo coronary artery lesions (311 lesions) | Posted | | Number | | participants | | Up to 30 days | Lesions | Participants | | ID | Title | Description |
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| OG000 | Treated With Presillion Stent | Patients treated with the Presillion stent in up to two de novo coronary artery lesions |
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| Secondary | Target Vessel Failure | Target vessel failure includes any target vessel revascularization as well as any MI or any cardiac death that cannot be clearly attributed to a non-target vessel. Target vessel failure will be reported when:
- MI occurs in territory not clearly attributed to a vessel other than the target vessel.
- Cardiac death not clearly due to a non-target vessel endpoint.
- Target vessel revascularization is performed.
| 309 patients treated with the Presillion stent in up to two de novo coronary artery lesions (311 lesions) | Posted | | Number | | participants | | Up to 30 days | Lesions | Participants | | ID | Title | Description |
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| OG000 | Treated With Presillion Stent | Patients treated with the Presillion stent in up to two de novo coronary artery lesions |
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| Secondary | Myocardial Infarction | A positive diagnosis of myocardial infarction is made when one of the following criteria is met:
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Typical rise and/or fall of biochemical markers of myocardial necrosis together with evidence of ischemia with at least one of the following:
- ischemic symptoms
- ECG changes indicative of ischemia (ST segment elevation or depression)
- Development of pathological Q waves in the ECG
- Imaging evidence of new an equivocal loss of viable myocardium or new regional wall motion abnormality
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Pathological findings of an acute myocardial infarction
| 309 patients treated with the Presillion stent in up to two de novo coronary artery lesions (311 lesions) | Posted | | Number | | participants | | Up to 30 days | Lesions | Participants | | ID | Title | Description |
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| OG000 | Treated With Presillion Stent | Patients treated with the Presillion stent in up to two de novo coronary artery lesions |
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| Secondary | Major Bleeding | | | Posted | | Number | | participants | | Up to 30 days | | | | ID | Title | Description |
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| OG000 | Treated With Presillion Stent | Patients treated with the Presillion stent in up to two de novo coronary artery lesions |
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| Secondary | Stroke | | | Posted | | Number | | participants | | Up to 30 days | | | | ID | Title | Description |
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| OG000 | Treated With Presillion Stent | Patients treated with the Presillion stent in up to two de novo coronary artery lesions |
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| Secondary | Stent Thrombosis | Thrombosis is defined as the formation of blood clot derived from aggregation of red cells or platelets obstructing the lumen of the vessel. | | Posted | | Number | | participants | | Up to 30 days | | | | ID | Title | Description |
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| OG000 | Treated With Presillion Stent | Patients treated with the Presillion stent in up to two de novo coronary artery lesions |
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| Secondary | Clinically Driven TLR | Target Lesion Revascularization (TLR) is defined as any clinically-driven repeat percutaneous intervention of the target lesion or bypass surgery of the target vessel | 303 patients treated with the Presillion stent in up to two de novo coronary artery lesions (308 lesions) | Posted | | Number | | participants | | up to 12 months | Lesions | Participants | | ID | Title | Description |
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| OG000 | Treated With Presillion Stent | Patients treated with the Presillion stent in up to two de novo coronary artery lesions |
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| Secondary | Clinically Driven TVR | Target vessel revascularization (TVR) is defined as any clinically driven (as defined for TLR) repeat percutaneous intervention of the target vessel or bypass surgery of the target vessel. | 303 patients treated with the Presillion stent in up to two de novo coronary artery lesions (308 lesions) | Posted | | Number | | participants | | Up to 12 months | Lesions | Participants | | ID | Title | Description |
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| OG000 | Treated With Presillion Stent | Patients treated with the Presillion stent in up to two de novo coronary artery lesions |
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| Secondary | Target Vessel Failure | Target vessel failure includes any target vessel revascularization as well as any MI or any cardiac death that cannot be clearly attributed to a non-target vessel. Target vessel failure will be reported when:
- MI occurs in territory not clearly attributed to a vessel other than the target vessel.
- Cardiac death not clearly due to a non-target vessel endpoint.
- Target vessel revascularization is performed.
| 303 patients treated with the Presillion stent in up to two de novo coronary artery lesions (308 lesions) | Posted | | Number | | participants | | Up to 12 months | Lesions | Participants | | ID | Title | Description |
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| OG000 | Treated With Presillion Stent | Patients treated with the Presillion stent in up to two de novo coronary artery lesions |
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| Secondary | Myocardial Infarction | A positive diagnosis of myocardial infarction is made when one of the following criteria is met:
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Typical rise and/or fall of biochemical markers of myocardial necrosis together with evidence of ischemia with at least one of the following:
- ischemic symptoms
- ECG changes indicative of ischemia (ST segment elevation or depression)
- Development of pathological Q waves in the ECG
- Imaging evidence of new an equivocal loss of viable myocardium or new regional wall motion abnormality
-
Pathological findings of an acute myocardial infarction
| 303 patients treated with the Presillion stent in up to two de novo coronary artery lesions (308 lesions) | Posted | | Number | | participants | | Up to 12 months | Lesions | Participants | | ID | Title | Description |
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| OG000 | Treated With Presillion Stent | Patients treated with the Presillion stent in up to two de novo coronary artery lesions |
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| Secondary | Major Bleeding | | | Posted | | Number | | participants | | Up to 12 months | | | | ID | Title | Description |
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| OG000 | Treated With Presillion Stent | Patients treated with the Presillion stent in up to two de novo coronary artery lesions |
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| Secondary | Stent Thrombosis | Thrombosis is defined as the formation of blood clot derived from aggregation of red cells or platelets obstructing the lumen of the vessel. | | Posted | | Number | | participants | | Up to 12 months | | | | ID | Title | Description |
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| OG000 | Treated With Presillion Stent | Patients treated with the Presillion stent in up to two de novo coronary artery lesions |
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| Secondary | Stroke | | | Posted | | Number | | participants | | Up to 12 months | | | | ID | Title | Description |
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| OG000 | Treated With Presillion Stent | Patients treated with the Presillion stent in up to two de novo coronary artery lesions |
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