AngioSculpt® Coronary Bifurcation Study

Not Applicable

Completed

Conditions: Coronary Artery Disease
Myocardial Ischemia

Registration Number: NCT00686647

Lead Sponsor: AngioScore, Inc.

Brief Summary: The purpose of this study is to evaluate a new angioplasty catheter, AngioSculpt® for the treatment of bifurcation lesions (blockages occurring at branch points) in coronary arteries.

Detailed Description: Background: Bifurcation lesions, which consist of a narrowing occurring at branch points of coronary arteries, typically involve both the main branch (parent vessel) and an adjacent side branch. These lesions pose a particularly challenging situation for angioplasty procedures due to the difficulty of covering both branches with stents and a higher rate of recurrence (restenosis). A new angioplasty scoring balloon catheter (AngioSculpt®) has recently been approved for the treatment of narrowings in coronary arteries. The AngioSculpt® catheter incorporates a nitinol device that consists of spiral wires that wrap around the balloon catheter. As the balloon inflates, the spiral wires score the lesion allowing the balloon to be more stable (avoid slippage) and may enlarge the narrowed sections of the artery with less pressure or risk of dissection (uncontrolled tearing of the inner lining of the artery wall commonly seen with conventional balloons).

Study Purpose: To demonstrate the safety and efficacy of the AngioSculpt® used in conjunction with coronary stents (implantable wire mesh tubes for scaffolding blocked arteries) for the treatment of coronary artery bifurcation narrowings and to compare these results with the historical outcomes associated with the use of conventional balloons and stents in the treatment of bifurcation lesions.

Study Design: A prospective, multi-center, non-randomized, single-arm study with results compared to a literature search derived historical control for conventional balloon angioplasty (OPC - Objective Performance Criteria). The intent of this study is to enroll and treat 100 patients at 8 U.S. interventional cardiology programs with clinical follow-up planned at 30 days and 9 months following the procedure.

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 93

Inclusion Criteria

At least 18 years of age and able to give informed consent.
Patients with significant (> 50% diameter stenosis) native coronary artery disease involving a bifurcation and the ostium of the side branch vessel (Medina class (x, x, 1)) including stable or unstable angina and silent ischemia.
Patients with lesions suitable for percutaneous coronary intervention (PCI).

Exclusion Criteria

Concomitant use of Rotablator, Cutting Balloon, or investigational coronary devices.
Additional planned coronary interventions for a non-target lesion within 9 months of the study procedure.
Left ventricular ejection fraction < 35%
Patients refusing or not candidates for emergency coronary artery bypass grafting (CABG)surgery
Uncontrolled severe hypertension (systolic BP >180 mm Hg or diastolic BP >110 mm Hg)
Patients who are not candidates for chronic treatment with aspirin or Clopidogrel/Ticlopidine
Severe renal failure with creatinine >2.0 mg/dL
Untreated pre-procedural hemoglobin <10 g/dL
Coagulopathy manifested by platelet count <100,000 or International Normalized ratio (INR) >2.0 (INR is only required in patients who have taken warfarin within 2 weeks of enrollment)
Women who are known or suspected to be pregnant
Patients in cardiogenic shock
Acute myocardial infarction (MI) within the past 72 hours, and/or elevated CPK (and abnormal Troponin-I) at the time of enrollment
Patients with a life expectancy of less than 1 year
Target main branch vessel < 2.5 mm in diameter
Target main branch lesion > 30 mm in length
Intended use of a bare metal stent (BMS) in the main branch
Target side branch vessel < 2.0 mm in diameter
Target side branch lesion > 15 mm in length
Target bifurcation angle > 90º (distal angle)
Totally obstructed target coronary arteries (TIMI 0 or 1 flow)
Target bifurcation lesion within a previously placed stent (i.e. in-stent restenosis (ISR))
Target bifurcation lesion within a surgical conduit (e.g. saphenous vein or internal mammary)
Target lesion demonstrating severe dissection prior to planned deployment of the AngioSculpt device
Unprotected Left Main diameter stenosis ≥ 50%
Visible thrombus (by angiography) at target lesion site
Coronary spasm in the absence of a significant stenosis
Patients who are concurrently participating in an investigational study when such participation could confound the treatment or outcomes of this study

Study & Design

Study Type: INTERVENTIONAL

Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Procedural Success	1 day	Defined as less than or equal to 30% diameter stenosis in the main branch and less than or equal to 70% diameter stenosis in the side branch at the conclusion of the procedure (including adjunctive stenting) in the absence of in-hospital major adverse cardiac events (MACE) \[cardiac death, myocardial infarction (MI), or target lesion revascularization (TLR\]

Secondary Outcome Measures

Name	Time	Method
Major Adverse Cardiovascular Events	30 days	cardiac death, myocardial infarction, or target lesion revascularization
Major Adverse Cardiac Events	9 months	cardiac death, myocardial infarction, or target lesion revascularization