A Clinical Trial to Assess the Elixir Medical LithiX Coronary Hertzian Contact Intravascular Lithotripsy Catheter

NCT ID: NCT05828173

Last Updated: 2025-03-06

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 60 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-04-27
• Study Completion Date: 2024-09-09

Brief Summary

The objective of the PINNACLE I Clinical Study is to assess safety and performance of the LithiX Coronary Hertzian Contact Intravascular Lithotripsy Catheter (LithiX Coronary HCIVLC; LithiX) to treat moderately to severely calcified coronary artery lesions by calcium fragmentation utilizing Hertzian contact stress from LithiX HCIVLC.

Detailed Description

This study is a prospective, multicenter, single-arm clinical study. Enrollment of up to 60 patients requiring percutaneous coronary intervention (PCI) on up to two de novo coronary artery lesions with reference vessel diameters ≥ 2.25 mm and ≤ 3.5 mm, and lesion lengths of ≤ 34 mm, with moderate to severe calcification.

The LithiX Coronary HCIVLC is a proprietary Hertzian contact intravascular lithotripsy catheter delivered through the coronary arterial system to visualize and treat calcified stenoses potentially resistant to full stent expansion. The LithiX Coronary HCIVLC consists of a semi-compliant balloon featuring multiple rows of stainless-steel hemispheres which are intended to atraumatically fragment calcium via Hertzian contact intravascular lithotripsy.

In the Optical Coherence Tomography (OCT) imaging subgroup, approximately 30 patients will undergo OCT imaging at pre-procedure, post-LithiX treatment, and the end of procedure following stent deployment.

Subjects will be followed through hospital discharge and will have clinical follow-up conducted by phone at 30 days and 6 months post-index procedure.

Conditions

Coronary Artery Disease

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

LithiX Coronary Hertzian Contact Intravascular Lithotripsy Treatment

Group Type: EXPERIMENTAL

LithiX Coronary Hertzian Contact Intravascular Lithotripsy Catheter (LithiX Coronary HCIVLC; LithiX)

Intervention Type: DEVICE

Vessel preparation of moderately to severely calcified coronary artery lesions prior to stenting allows for full stent expansion and apposition to the vessel wall

Interventions

LithiX Coronary Hertzian Contact Intravascular Lithotripsy Catheter (LithiX Coronary HCIVLC; LithiX)

Vessel preparation of moderately to severely calcified coronary artery lesions prior to stenting allows for full stent expansion and apposition to the vessel wall

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

1. Subject is ≥ 18 years of age.

2. Subject or a legally authorized representative must provide written informed consent prior to any study related procedures.

3. Subject must agree not to participate in any other clinical study during the course of the study that would interfere with the endpoints of this study.

4. Subjects must have a single or double vessel coronary artery disease (CAD) and clinical evidence of ischemic heart disease, such as CAD, silent ischemia, stable / unstable angina, and NSTEMI if biomarkers are stable or falling at time of inclusion.

1. Subject must have de novo lesion(s) in native coronary arteries suitable for percutaneous coronary intervention.

2. Up to 2 de novo coronary artery lesions in separate epicardial vessels, which are moderately to severely calcified, meeting all of the following criteria visually assessed by angiography:

• ≥70% diameter stenosis by visual estimation
• reference vessel diameters of 2.25 mm - 3.5 mm
• lesion length of ≤ 34 mm
• TIMI flow ≥ 1 at baseline

3. Any non-target lesion must be located in different coronary artery from a target lesion. Treatment of non-target lesion, if any, must be completed prior to treatment of target lesion and must be deemed a clinical angiographic success as visually assessed by the physician.

Exclusion Criteria

1. Subject with a known hypersensitivity or contraindication to aspirin, heparin, bivalirudin, anti-platelet medications, or sensitivity to contrast media which cannot be adequately pre-medicated.

2. Subject with known diagnosis of STEMI at index presentation or within 7 days of study screening.

3. Patient refusing or not a candidate for emergency coronary artery bypass grafting (CABG) surgery.

4. Subject with known pregnancy or is nursing. Women of child-bearing potential should have a documented negative pregnancy test within 7 days before index procedure.

5. Planned use of atherectomy, laser, lithoplasty, thrombectomy, scoring or cutting balloon, or any investigational device other than LithiX in the target lesion during the index procedure.

6. Patients on renal dialysis or with known eGFR < 30 ml/min.

7. NYHA class III or IV heart failure.

8. Patient has active systemic infection.

9. Cerebrovascular accident (CVA) or transient ischemic attach (TIA) within the past 6 months.

10. Active peptic ulcer or active gastrointestinal (GI) bleeding within the past 6 months.

11. Subject has a known left ventricular ejection fraction (LVEF) <30% (LVEF may be obtained at the time of the index procedure if the value is unknown, if necessary).

12. Subject is a member of a vulnerable population as defined GCP E6, including individuals with mental disability, persons in nursing homes, children, impoverished persons, persons in emergency situations, homeless persons, nomads, refugees, and those incapable of giving informed consent. Vulnerable populations also may include members of a group with a hierarchical structure such as university students, subordinate hospital and laboratory personnel, employees of the Sponsor, members of the armed forces, and persons kept in detention.

1. More than two target lesions or more than 1 target and 1 non-target lesion requiring treatment.

2. Extreme angulation (90º or greater) proximal to or within the target lesion.

3. Previous percutaneous intervention of lesions in a target vessel (including side branches) conducted within 6 months before the study procedure, or any prior lesion treated within 10 mm (proximal or distal) from the current target lesion.

4. Previous percutaneous intervention of lesions in a non-target vessel (including side branches) conducted within 30 days before the study procedure.

5. Angiographic evidence of a target lesion dissection prior to LithiX Hertzian Contact Lithotripsy.

6. Visible thrombus (by angiography) at target lesion site.

7. Unprotected left main coronary artery disease (Greater than 50% diameter stenosis).

8. Target lesion is located in a native vessel distal to anastomosis with a saphenous vein graft or LIMA/RIMA bypass.

9. Evidence of aneurysm in target vessel.

10. Coronary artery spasm of the target vessel in the absence of a significant stenosis.

11. Target lesion involves a bifurcation requiring treatment with more than one stent or pre-dilatation of a side branch >2.0 mm in diameter

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Elixir Medical Corporation

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Stefan Verheye, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

ZNA Middelheim, Antwerp, Belgium

Johan Bennett, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Universitaire Ziekenhuizen Leuven, Leuven, Belgium

Locations

ZNA Middelheim

Antwerp, , Belgium

Ziekenhuis Oost-Limburg, Campus Sint Jan

Genk, , Belgium

Jessa Ziekenhuis

Hasselt, , Belgium

Universitaire Ziekenhuizen Leuven

Leuven, , Belgium

Meander Medical Centre

Amersfoort, , Netherlands

Catharina Ziekenhuis

Eindhoven, , Netherlands

Maasstad Ziekenhuis

Rotterdam, , Netherlands

Countries

Belgium; Netherlands

Other Identifiers

ELX-CL-2202

Identifier Type: -

Identifier Source: org_study_id