| Primary | Composite Endpoint of Cardiac Death/TV-MI/CI-TLR (TLF) | Target lesion failure (TLF) is the composite of any of the following adverse events: Cardiac death, target vessel myocardial infarction (TV-MI) (per Protocol definition), Clinically indicated target lesion revascularization (CI-TLR) | Full Analysis Set (FAS population) | Posted | | Number | | percentage of participants | | 9 Months | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS |
| | | Title | Denominators | Categories |
|---|
| | |
| |
| Secondary | Device Success (Lesion Based Analysis, Only for XIENCE PRIME SV) | Device success is achievement final in-stent residual diameter stenosis of < 50% (by QCA). If adjunct treatment devices other than protocol defined device is used for target lesion treatment, malfunction of the investigational device occurring during the index procedure, are not regarded as device success. Use of a bail-out stent is still regarded as device success unless a device malfunction has occured. If QCA %DS is not available, the data is not included in analyses. | Intent to Treat Population (ITT) | Posted | | Number | 95% Confidence Interval | percentage of participants | | The period during an in-hospital stay of less than or equal to 7 days post index procedure. | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS |
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| Secondary | Procedural Success(Subject Base Analysis) | Procedure success is defined as achievement of a final in-stent diameter stenosis of < 50% (by QCA) using the investigational device (AVJ-09-385), without the occurrence MACE during the hospital stay (up to 7 days if a subject still in the hospital). If QCA %DS is not available, the data is not included in analyses. | | Posted | | Number | 95% Confidence Interval | percentage of participants | | The period during an in-hospital stay of less than or equal to 7 days post index procedure. | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS | XIENCE PRIME SV EECSS EECSS : Patients receiving XIENCE PRIME SV EECSS |
| |
| Secondary | Percent Diameter Stenosis (%DS), In-segment, In-stent, Proximal and Distal | IN-STENT is defined as within the margins of the stent. IN-SEGMENT is defined as within the margins of the stent and 5 mm proximal and 5 mm distal to the stent. PROXIMAL is defined as within 5 mm of healthy tissue proximal to stent placement DISTAL is defined as within 5 mm of healthy tissue distal to stent placement | Full Analysis Set (FAS population) | Posted | | Mean | Standard Deviation | percentage of DS | | 8 months | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS %DS In-segment | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG001 | XIENCE PRIME SV EECSS %DS In-stent | XIENCE PRIME SV EECSS: Patients receiving XIENCE PRIME SV EECSS | | OG002 | XIENCE PRIME SV EECSS %DS Proximal | XIENCE PRIME SV EECSS: Patients receiving XIENCE PRIME SV EECSS | | OG003 | XIENCE PRIME SV EECSS %DS Distal | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS |
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| Secondary | Late Loss (LL), In-segment, In-stent, Proximal and Distal | LATE LOSS (LL) calculated as MINIMUM LUMEN DIAMETER [MLD] post-procedure MINUS MLD at follow-up: In-segment Late Loss: in-segment MLD post-procedure - in segment MLD at follow-up In-stent Late Loss: in-stent MLD post-procedure - in-stent MLD at follow-up Proximal Late Loss: proximal MLD post-procedure - proximal MLD at follow-up (proximal defined as within 5 mm of healthy tissue proximal to stent placement) Distal Late Loss: distal MLD post-procedure - distal MLD at follow-up (distal defined as within 5 mm of healthy tissue distal to stent placement) | Full Analysis Set (FAS population) | Posted | | Mean | Standard Deviation | mm | | 8 months | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS LL In-segment | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG001 | XIENCE PRIME SV EECSS LL In-stent | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG002 | XIENCE PRIME SV EECSS LL Proximal | XIENCE PRIME SV EECSS: Patients receivingXIENCE PRIME SV EECSS | | OG003 |
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| Secondary | Angiographic Binary Restenosis (ABR), In-segment, In-stent, Proximal and Distal | IN-STENT is defined as within the margins of the stent. IN-SEGMENT is defined as within the margins of the stent and 5 mm proximal and 5 mm distal to the stent. PROXIMAL is defined as within 5 mm of healthy tissue proximal to stent placement DISTAL is defined as within 5 mm of healthy tissue distal to stent placement | Full Analysis Set (FAS population) | Posted | | Number | 95% Confidence Interval | percentage of participants | | 8 months | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS ABR In-segment | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG001 | XIENCE PRIME SV EECSS ABR In-stent | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG002 | XIENCE PRIME SV EECSS ABR Proximal | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG003 | XIENCE PRIME SV EECSS ABR Distal | XIENCE PRIME SV EECSS : Patients receivingXIENCE PRIME SV EECSS |
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| Secondary | Death (Cardiac, Vascular, Non-Cardiovascular, Per ARC Definition) | DEATH (Per ARC Circulation 2007; 115: 2344-2351) All deaths are considered cardiac unless an unequivocal non-cardiac cause can be established. Specifically, any unexpected death even in patients with coexisting potentially fatal non-cardiac disease (e.g. cancer, infection) should be classified as cardiac. | | Posted | | Number | | percentage of participants | | 1 month | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS - Cardiac | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG001 | XIENCE PRIME SV EECSS - Vascular | XIENCE PRIME SV EECSS : Patients receiving AXIENCE PRIME SV EECSS | | OG002 | XIENCE PRIME SV EECSS - Non-Cardiovascular | XIENCE PRIME SV EECSS : Patients receivingXIENCE PRIME SV EECSS |
| |
| Secondary | Death (Cardiac, Vascular, Non-Cardiovascular, Per ARC Definition) | DEATH (Per ARC Circulation 2007; 115: 2344-2351) All deaths are considered cardiac unless an unequivocal non-cardiac cause can be established. Specifically, any unexpected death even in patients with coexisting potentially fatal non-cardiac disease (e.g. cancer, infection) should be classified as cardiac. | Full Analysis Set (FAS population) | Posted | | Number | | percentage of participants | | 9 months | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS - All Death Per ARC | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG001 | XIENCE PRIME SV EECSS - Cardiac Death Per ARC | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG002 | XIENCE PRIME SV EECSS - Vascular Death Per ARC | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG003 | XIENCE PRIME SV EECSS - Non-Cardiovascular Death Per ARC | XIENCE PRIME SV EECSS : Patients receiving AXIENCE PRIME SV EECSS |
|
| Secondary | Myocardial Infarction (MI: QMI and NQMI, Both Per SPIRIT III Protocol and Per ARC Definitions) | Definitions in SPIRIT III Study: Q wave MI: Development of new, pathological Q wave on the ECG Non-Q wave MI: Elevation of CK levels to >=two times the upper limit of normal (ULN) with elevated CK-MB in the absence of new pathological Q waves Per ARC definition as published in 'Academic Research Consortium., Clinical end points in coronary stent trials: a case for standardized definitions.' Circulation 2007; 115: 2344-2351 | Full Analysis Set (FAS population) | Posted | | Number | | percentage of participants | | 1 month | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS - QMI Per Protocol | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG001 | XIENCE PRIME SV EECSS - NQMI Per Protocol | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG002 | XIENCE PRIME SV EECSS - QMI Per ARC Definitions | XIENCE PRIME SV EECSS : Patients receivingXIENCE PRIME SV EECSS | | OG003 | XIENCE PRIME SV EECSS - NQMI Per ARC Definitions |
|
| Secondary | Myocardial Infarction (MI: QMI and NQMI, Both Per SPIRIT III Protocol and Per ARC Definitions) | Definitions in SPIRIT III Study: Q wave MI: Development of new, pathological Q wave on the ECG Non-Q wave MI: Elevation of CK levels to >=two times the upper limit of normal (ULN) with elevated CK-MB in the absence of new pathological Q waves Per ARC definition as published in 'Academic Research Consortium., Clinical end points in coronary stent trials: a case for standardized definitions.' Circulation 2007; 115: 2344-2351 | Full Analysis Set (FAS population) | Posted | | Number | | percentage of participants | | 9 months | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS - QMI Per Protocol | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG001 | XIENCE PRIME SV EECSS - NQMI Per Protocol | XIENCE PRIME SV EECSS : Patients receivingXIENCE PRIME SV EECSS | | OG002 | XIENCE PRIME SV EECSS - QMI Per ARC | XIENCE PRIME SV EECSS: Patients receiving XIENCE PRIME SV EECSS | | OG003 | XIENCE PRIME SV EECSS - NQMI Per ARC |
|
| Secondary | Myocardial Infarction (MI: QMI and NQMI, Both Per SPIRIT III Protocol and Per ARC Definitions) Attributable to Target Vessel (TV-MI) | Definitions in SPIRIT III Study: Q wave MI: Development of new, pathological Q wave on the ECG Non-Q wave MI: Elevation of CK levels to >=two times the upper limit of normal (ULN) with elevated CK-MB in the absence of new pathological Q waves Per ARC definition as published in 'Academic Research Consortium., Clinical end points in coronary stent trials: a case for standardized definitions.' Circulation 2007; 115: 2344-2351 | Full Analysis Set (FAS population) | Posted | | Number | | percentage of participants | | 1 month | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS- TV-QMI Per Protocol | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG001 | XIENCE PRIME SV EECSS - TV-NQMI Per Protocol | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG002 | XIENCE PRIME SV EECSS - TV-QMI Per ARC | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG003 | XIENCE PRIME SV EECSS - TV-NQMI Per ARC |
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| Secondary | Myocardial Infarction (MI: QMI and NQMI, Both Per SPIRIT III Protocol and Per ARC Definitions) Attributable to Target Vessel (TV-MI) | Definitions in SPIRIT III Study: Q wave MI: Development of new, pathological Q wave on the ECG Non-Q wave MI: Elevation of CK levels to >=two times the upper limit of normal (ULN) with elevated CK-MB in the absence of new pathological Q waves Per ARC definition as published in 'Academic Research Consortium., Clinical end points in coronary stent trials: a case for standardized definitions.' Circulation 2007; 115: 2344-2351 | Full Analysis Set (FAS population) | Posted | | Number | | percentage of participants | | 9 months | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS - TV-QMI Per Protocol | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG001 | XIENCE PRIME SV EECSS - TV-NQMI Per Protocol | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG002 | XIENCE PRIME SV EECSS - TV-QMI Per ARC | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG003 | XIENCE PRIME SV EECSS - TV-NQMI Per ARC |
|
| Secondary | Myocardial Infarction (MI: QMI and NQMI, Both Per SPIRIT III Protocol and Per ARC Definitions) Not Attributable to Target Vessel (NTV-MI) | Definitions in SPIRIT III Study: Q wave MI: Development of new, pathological Q wave on the ECG Non-Q wave MI: Elevation of CK levels to >=two times the upper limit of normal (ULN) with elevated CK-MB in the absence of new pathological Q waves Per ARC definition as published in 'Academic Research Consortium., Clinical end points in coronary stent trials: a case for standardized definitions.' Circulation 2007; 115: 2344-2351 | | Posted | | Number | | percentage of participants | | 1 month | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS Non-Target Vessel QMI Per Protocol | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG001 | XIENCE PRIME SV EECSS Non-Target Vessel NQMI Per Protocol | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG002 | XIENCE PRIME SV EECSS Non-Target Vessel QMI Per ARC | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG003 |
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| Secondary | Myocardial Infarction (MI: QMI and NQMI, Both Per SPIRIT III Protocol and Per ARC Definitions) Not Attributable to Target Vessel (NTV-MI) | Definitions in SPIRIT III Study: Q wave MI: Development of new, pathological Q wave on the ECG Non-Q wave MI: Elevation of CK levels to >=two times the upper limit of normal (ULN) with elevated CK-MB in the absence of new pathological Q waves Per ARC definition as published in 'Academic Research Consortium., Clinical end points in coronary stent trials: a case for standardized definitions.' Circulation 2007; 115: 2344-2351 | Full Analysis Set (FAS population) | Posted | | Number | | percentage of participants | | 9 months | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS - NTV-QMI Per Protocol | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG001 | XIENCE PRIME SV EECSS - NTV-NQMI Per Protocol | XIENCE PRIME SV EECSS: Patients receiving XIENCE PRIME SV EECSS | | OG002 | XIENCE PRIME SV EECSS - NTV-QMI Per ARC | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG003 | XIENCE PRIME SV EECSS - NTV-NQMI Per ARC |
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| Secondary | Target Lesion Revascularization (TLR, Per ARC Definition) | Any revascularization for in-segment restenosis will be considered TLR."Segment" is defined as the area within the margins of the stent and 5 mm proximal and 5 mm distal to the stent. Revascularization was considered clinically indicated if there was >70% diameter stenosis on angiography or >50% stenosis together with a positive stress test or ischaemic symptoms. | Full analysis set (FAS) population | Posted | | Number | | percentage of participants | | 1 month | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS |
| |
| Secondary | Target Lesion Revascularization (TLR, Per ARC Definition) | Any revascularization for in-segment restenosis will be considered TLR. "Segment" is defined as the area within the margins of the stent and 5 mm proximal and 5 mm distal to the stent. Revascularization was considered clinically indicated if there was >70% diameter stenosis on angiography or >50% stenosis together with a positive stress test or ischaemic symptoms. | | Posted | | Number | | percentage of participants | | 9 months | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS |
| |
| Secondary | Target Lesion Revascularization (TLR, Per ARC Definition) Clinically-indicated TLR (CI-TLR) | Any revascularization for in-segment restenosis will be considered TLR. "Segment" is defined as the area within the margins of the stent and 5 mm proximal and 5 mm distal to the stent. Revascularization was considered clinically indicated if there was >70% diameter stenosis on angiography or >50% stenosis together with a positive stress test or ischaemic symptoms. | Full analysis set (FAS) population | Posted | | Number | | percentage of participants | | 1 month | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS |
| |
| Secondary | Target Lesion Revascularization (TLR, Per ARC Definition) Clinically-indicated TLR (CI-TLR) | Any revascularization for in-segment restenosis will be considered TLR. "Segment" is defined as the area within the margins of the stent and 5 mm proximal and 5 mm distal to the stent. Revascularization was considered clinically indicated if there was >70% diameter stenosis on angiography or >50% stenosis together with a positive stress test or ischaemic symptoms. | Full Analysis Set (FAS population) | Posted | | Number | | percentage of participants | | 9 months | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS |
| |
| Secondary | Target Lesion Revascularization (TLR, Per ARC Definition) Not Clinically-indicated TLR (NCI-TLR) | Any revascularization for in-segment restenosis will be considered TLR. "Segment" is defined as the area within the margins of the stent and 5 mm proximal and 5 mm distal to the stent. Revascularization was considered clinically indicated if there was >70% diameter stenosis on angiography or >50% stenosis together with a positive stress test or ischaemic symptoms. | Full analysis set (FAS) population | Posted | | Number | | percentage of participants | | 1 month | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS | XIENCE PRIME SV EECSS: Patients receiving XIENCE PRIME SV EECSS |
| |
| Secondary | Target Lesion Revascularization (TLR, Per ARC Definition) Not Clinically-indicated TLR (NCI-TLR) | Any revascularization for in-segment restenosis will be considered TLR. "Segment" is defined as the area within the margins of the stent and 5 mm proximal and 5 mm distal to the stent. Revascularization was considered clinically indicated if there was >70% diameter stenosis on angiography or >50% stenosis together with a positive stress test or ischaemic symptoms. | | Posted | | Number | | percentage of participants | | 9 months | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS |
| |
| Secondary | Target Vessel Revascularization (TVR, Per ARC Definition) | TVR is defined as any repeat percutaneous intervention or surgical bypass of any segment of the target vessel. The target vessel is defined as the entire major coronary vessel proximal and distal to the target lesion which includes upstream and downstream branches and the target lesion itself. Revascularization was considered clinically indicated if there was >70% diameter stenosis on angiography or >50% stenosis together with a positive stress test or ischaemic symptoms. | | Posted | | Number | | percentage of participants | | 1 month | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS |
| |
| Secondary | Target Vessel Revascularization (TVR, Per ARC Definition) | TVR is defined as any repeat percutaneous intervention or surgical bypass of any segment of the target vessel. The target vessel is defined as the entire major coronary vessel proximal and distal to the target lesion which includes upstream and downstream branches and the target lesion itself. Revascularization was considered clinically indicated if there was >70% diameter stenosis on angiography or >50% stenosis together with a positive stress test or ischaemic symptoms. | | Posted | | Number | | percentage of participants | | 9 months | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS | XIENCE PRIME SV EECSS: Patients receiving XIENCE PRIME SV EECSS |
| |
| Secondary | Target Vessel Revascularization (TVR, Per ARC Definition) Clinically-indicated TVR (CI-TVR) | TVR is defined as any repeat percutaneous intervention or surgical bypass of any segment of the target vessel. The target vessel is defined as the entire major coronary vessel proximal and distal to the target lesion which includes upstream and downstream branches and the target lesion itself. Revascularization was considered clinically indicated if there was >70% diameter stenosis on angiography or >50% stenosis together with a positive stress test or ischaemic symptoms. | Full analysis set (FAS) population | Posted | | Number | | percentage of participants | | 1 month | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS |
| |
| Secondary | Target Vessel Revascularization (TVR, Per ARC Definition) Clinically-indicated TVR (CI-TVR) | TVR is defined as any repeat percutaneous intervention or surgical bypass of any segment of the target vessel. The target vessel is defined as the entire major coronary vessel proximal and distal to the target lesion which includes upstream and downstream branches and the target lesion itself. Revascularization was considered clinically indicated if there was >70% diameter stenosis on angiography or >50% stenosis together with a positive stress test or ischaemic symptoms. | Full Analysis Set (FAS population) | Posted | | Number | | percentage of participants | | 9 months | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS | XIENCE PRIME SV EECSS: Patients receiving XIENCE PRIME SV EECSS |
| |
| Secondary | Target Vessel Revascularization (TVR, Per ARC Definition) Not Clinically-indicated TVR (NCI-TVR) | TVR is defined as any repeat percutaneous intervention or surgical bypass of any segment of the target vessel. The target vessel is defined as the entire major coronary vessel proximal and distal to the target lesion which includes upstream and downstream branches and the target lesion itself. Revascularization was considered clinically indicated if there was >70% diameter stenosis on angiography or >50% stenosis together with a positive stress test or ischaemic symptoms. | Full Analysis Set (FAS population) | Posted | | Number | | percentage of participants | | 1 month | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS |
| |
| Secondary | Target Vessel Revascularization (TVR, Per ARC Definition) Not Clinically-indicated TVR (NCI-TVR) | TVR is defined as any repeat percutaneous intervention or surgical bypass of any segment of the target vessel. The target vessel is defined as the entire major coronary vessel proximal and distal to the target lesion which includes upstream and downstream branches and the target lesion itself. Revascularization was considered clinically indicated if there was >70% diameter stenosis on angiography or >50% stenosis together with a positive stress test or ischaemic symptoms. | Full Analysis Set (FAS population) | Posted | | Number | | percentage of participants | | 9 months | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS |
| |
| Secondary | Composite Endpoint of Cardiac Death/All MI | | Full Analysis Set (FAS population) | Posted | | Number | | percentage of participants | | 1 month | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS |
| | | Title | Denominators | Categories |
|---|
|
|
| Secondary | Composite Endpoint of Cardiac Death/All MI | | Full Analysis Set (FAS population) | Posted | | Number | | percentage of participants | | 9 months | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS |
| | | Title | Denominators | Categories |
|---|
|
|
| Secondary | Composite Endpoint of All Death/All MI/All Revascularization (DMR) | DMR event (all death, all MI (per protocol or per ARC), all revascularization, respectively). | Full Analysis Set (FAS population) | Posted | | Number | | percentage of participants | | 1 month | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS |
| | |
| Secondary | Composite Endpoint of All Death/All MI/All Revascularization (DMR) | DMR event (all death, all MI (per protocol or per ARC), all revascularization, respectively). | Full Analysis Set (FAS population) | Posted | | Number | | percentage of participants | | 9 months | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS | XIENCE PRIME SV EECSS: Patients receiving XIENCE PRIME SV EECSS |
| | |
| Secondary | Composite Endpoint of Cardiac Death/TV-MI/CI-TLR (TLF) | Target lesion failure (TLF) is defined as a composite of cardiac death, target-vessel related myocardial infarction (TV-MI) and clinically-indicated target lesion revascularization (CI-TLR). | | Posted | | Number | | percentage of participants | | 1 month | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS | XIENCE PRIME SV EECSS: Patients receiving XIENCE PRIME SV EECSS |
| | |
| Secondary | Composite Endpoint of Cardiac Death/All MI/CI-TLR (MACE) | Major adverse cardiac events (MACE) is defined as the composite of cardiac death, all myocardial-infarction, and clinically-indicated target lesion revascularization (CI-TLR). | Full Analysis Set (FAS population) | Posted | | Number | | percentage of participants | | 1 month | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS | XIENCE PRIME SV EECSS: Patients receiving XIENCE PRIME SV EECSS |
| | |
| Secondary | Composite Endpoint of Cardiac Death, All MI and CI-TLR (MACE) | Major adverse cardiac events (MACE) is defined as the composite of cardiac death, all myocardial-infarction, and clinically-indicated target lesion revascularization (CI-TLR). | | Posted | | Number | | percentage of participants | | 9 months | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS | XIENCE PRIME SV EECSS: Patients receiving XIENCE PRIME SV EECSS |
| | |
| Secondary | All Coronary Revascularization | | Full Analysis Set (FAS population) | Posted | | Number | | percentage of participants | | 1 months | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS | XIENCE PRIME SV EECSS: Patients receiving XIENCE PRIME SV EECSS |
| | | Title | Denominators | Categories |
|---|
|
|
| Secondary | All Coronary Revascularization | | | Posted | | Number | | percentage of participants | | 9 months | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS |
| | | Title | Denominators | Categories |
|---|
|
|
| Secondary | Acute Stent Thrombosis | Stent thrombosis (ST) was defined according to the ARC guidelines as follows: definite: acute coronary syndrome and angiographic or pathological confirmation of ST; probable: unexplained death ≤30 days or target vessel MI without angiographic information; and possible: unexplained death >30 days after stent placement." | | Posted | | Number | | percentage of participants | | <24 hours | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS - ST Definite | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG001 | XIENCE PRIME SV EECSS - ST Probable | XIENCE PRIME SV EECSS: Patients receiving XIENCE PRIME SV EECSS | | OG002 | XIENCE PRIME SV EECSS - ST Possible | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG003 | XIENCE PRIME SV EECSS - ST Definite/Probable | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS |
|
| Secondary | Subacute Stent Thrombosis | Stent thrombosis was defined according to the ARC guidelines as follows: definite: acute coronary syndrome and angiographic or pathological confirmation of ST; probable: unexplained death ≤30 days or target vessel MI without angiographic information; and possible: unexplained death >30 days after stent placement." | | Posted | | Number | | percentage of participants | | 1-30 days | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS - ST Definite | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG001 | XIENCE PRIME SV EECSS - ST Probable | XIENCE PRIME SV EECSS: Patients receiving XIENCE PRIME SV EECSS | | OG002 | XIENCE PRIME SV EECSS - ST Possible | XIENCE PRIME SV EECSS: Patients receiving XIENCE PRIME SV EECSS | | OG003 | XIENCE PRIME SV EECSS - ST Definite/Probable | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS |
|
| Secondary | Acute/Subacute Stent Thrombosis | Stent thrombosis was defined according to the ARC guidelines as follows: definite: acute coronary syndrome and angiographic or pathological confirmation of ST; probable: unexplained death ≤30 days or target vessel MI without angiographic information; and possible: unexplained death >30 days after stent placement." | | Posted | | Number | | percentage of participants | | 0-30 days | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS - ST Definite | XIENCE PRIME SV EECSS: Patients receiving XIENCE PRIME SV EECSS | | OG001 | XIENCE PRIME SV EECSS - ST Probable | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG002 | XIENCE PRIME SV EECSS - ST Possible | XIENCE PRIME SV EECSS: Patients receiving XIENCE PRIME SV EECSS | | OG003 | XIENCE PRIME SV EECSS - ST Definite/Probable | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS |
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| Secondary | Late Stent Thrombosis | Stent thrombosis was defined according to the ARC guidelines as follows: definite: acute coronary syndrome and angiographic or pathological confirmation of ST; probable: unexplained death ≤30 days or target vessel MI without angiographic information; and possible: unexplained death >30 days after stent placement." | | Posted | | Number | | percentage of participants | | 31 - 298 days | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS - ST Definite | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG001 | XIENCE PRIME SV EECSS- ST Probable | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG002 | XIENCE PRIME SV EECSS - ST Possible | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG003 | XIENCE PRIME SV EECSS - ST Definite/Probable | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS |
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| Secondary | Overall Stent Thrombosis | Stent thrombosis was defined according to the ARC guidelines as follows: definite: acute coronary syndrome and angiographic or pathological confirmation of ST; probable: unexplained death ≤30 days or target vessel MI without angiographic information; and possible: unexplained death >30 days after stent placement." | | Posted | | Number | | percentage of participants | | 0 - 298 days | | | | ID | Title | Description |
|---|
| OG000 | XIENCE PRIME SV EECSS - ST Definite | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG001 | XIENCE PRIME SV EECSS - ST Probable | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG002 | XIENCE PRIME SV EECSS - ST Possible | XIENCE PRIME SV EECSS: Small Vessel Everolimus Eluting Coronary Stent System XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS | | OG003 | XIENCE PRIME SV EECSS - ST Definite/Probable | XIENCE PRIME SV EECSS : Patients receiving XIENCE PRIME SV EECSS |
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