Bivalirudin Plus Stenting in Long Lesion to Avoid Periprocedural Myocardial Necrosis Trial
Status:
Unknown status
Trial end date:
2012-10-01
Target enrollment:
Participant gender:
Summary
Background:
Randomized trials show improved outcomes among acute coronary syndrome (ACS) patients treated
with Bivalirudin1. Optimal antithrombotic treatment in patients undergoing percutaneous
coronary intervention (PCI) is crucial to balance the risk of post-PCI bleeding versus
ischemic complications2. Bivalirudin, a direct thrombin inhibitor has been extensively
investigated as an intra-procedural antithrombotic therapy in patients with stable angina,
Non ST-segment elevation acute coronary syndrome (NSTE-ACS), and ST-segment elevation
myocardial infarction (STEMI). Bivalirudin, when used with or without glycoprotein IIb/IIIa
inhibitors (GPI) during PCI has been found to be superior to Unfractionated heparin (UFH)
with or without GPI in reducing 30-day bleeding complications without significant increase in
the rate of ischemic events3-5.
Moreover,after otherwise successful PCI,an increase in cardiac biomarkers has been shown to
occur in 5% to 30% of patients6. Recent studies have focused their attention onthe reduction
of infarct size and the incidence of periprocedural (type IVa) myocardial infarction
(PMI)after elective PCI7-8. Therefore, we will perform a single-center, prospective and
randomized study to assess if Bivalirudin versus UFHis effective in preventing elevation of
biomarkers of MI after coronary stent implantation in patients already treated with aspirin
and clopidogrel,with anatomically complex lesion.
Objective:
to assess the safety and efficacy of routine usage of the Bivalirudin vs UFH in patients with
coronary artery disease (CAD), after stent implantation in coronary long lesions, to avoid
periprocedural myocardial necrosis.
Setting:
Single-center, spontaneous, prospective, randomized 1:1 study of Bivalirudin infusion vs UFH
in the setting of CAD, after PCI with stenting incoronary long lesions.
Comparison: Bivalirudin vs UFH, in preventing elevation of biomarkers of MI after coronary
stent implantation in patients already treated with aspirin and clopidogrel, with
anatomically complex lesion.
Population:Patients with diffuse CAD undergoing percutaneous treatment on a native coronary
vessel with planned implantation stents in overlapping with a total stent length >33 mm for
long coronary lesions in vessels with a reference vessel diameter 2.25-4.0 mm.
Assessment Following the procedure, blood samples for CK, CK-MB and Troponin will be
collected at 6,12 and 24 h post PCI. CK-MB values will be considered abnormal if they will
elevate above the upper limit of normal (ULN). This is set at 6 mg/L by our local laboratory.
If the first blood sample showed a CK-MB level ≥18 mg/L (≥3 times upper normal limit), a
second blood sample would be drawn every 8 h later until a downward trend will be observed.
For patients with two or more blood samples drawn, the peak CK-MB level will be used for
analysis.
End-points:
The primary end-point of this study will be the incidence of periprocedural myonecrosis that
was defined as a peak post-procedural CK-MB elevation > 1 time the upper limit of normal
(ULN) alone or associated with chest pain or ST-segment or T-wave abnormalities, in patients
undergoing non-urgent PCI.
Secondary end-points will be the rate of MACCE (major adverse cerebro-cardiovascular events,
ie the composite of death, myocardial infarction [defined according to the Academic Research
Consortium statement], target vessel revascularization or stroke), the rate of major
bleedings (Bleeding Academic Consortium [BARC] 3-5), minor bleedings (BARC 2), and the rate
of NACE (net adverse clinical events, ie the composite of MACCE and major bleedings) at 30
days, 6 and 12 month follow-up. Adverse events will be determined by telephone interview
and/or medical record review. Clinical follow-up: telephone-based interviews and office-based
direct visits will be performed at 1, 6 and 12 months, respectively, for end-point
adjudication.
Sample size and statistical analysis: Given an expected rate of abnormal post-procedural peak
CK-MB > 1 x ULM of 48% (based on results of the INSTANT trial) for the control group and 29%
for the experimental group (thus a 40% relative risk reduction), aiming for a 0.05 alpha and
0.80 power, a total of 204 patients will need to be enrolled (102 patients per group).