The Value of IVL Compared To OPN Non-Compliant Balloons for Treatment of RefractorY Coronary Lesions (VICTORY) Trial
The Value of IVL Compared To OPN Non-Compliant Balloons for Treatment of RefractorY Coronary Lesions (VICTORY) Trial - A Randomized, Multicenter, Non-inferiority Comparison of Shockwave Intravascular Lithotripsy (IVL) and the OPN Non-compliant Balloon for Treatment of Calcified and Refractory Coronary Lesions
Luzerner Kantonsspital
280 participants
Nov 22, 2022
INTERVENTIONAL
Conditions
Summary
Percutaneous coronary intervention (PCI) with drug-eluting stent (DES) implantation has become the dominant treatment strategy for patients with acute and chronic coronary artery disease (CAD) requiring revascularization. Nonetheless, PCI with stent implantation has some limitations and especially patients with severely calcified coronary lesions (approximately 10-20% of all patients with CAD) have an elevated risk for adverse outcomes, including target lesion failure (TLF) and stent thrombosis (ST). Several dedicated PCI devices have been developed for treatment of severely calcified lesions. Whereas especially two of them have shown promising results in smaller, prospective studies. First, the super high-pressure NC PCI balloon (OPN™ NC, SIS Medical AG, Frauenfeld, Switzerland) has been shown to represent an effective and safe device for lesion preparation. Second, the lately introduced Shockwave intravascular lithotripsy (IVL)™ balloon catheter (Shockwave Medical, Santa Clara, CA, USA) appears to be a safe and efficient alternative device for treatment of calcified coronary lesions. However, it remains unknown, if the OPN™ NC balloon is non-inferior to to IVL regarding lesion preparation and completeness of stent expansion in severely calcified lesions.
Eligibility
Inclusion Criteria16
- Age ≥18 years and consentable;
- Acute or chronic coronary artery disease with ischemia related symptoms (e.g. angina) and/or evidence of myocardial ischemia (e.g. FFR/ iFR, CMR, SPECT or PET-CT);
- Angiographically-proven coronary artery disease;
- Lesions in non-target vessels requiring PCI may be treated either
- prior to the study procedure if the procedure was unsuccessful or complicated; or
- in the same session if feasible and safe for the patient, otherwise a staged PCI procedure for non-target vessels may be considered;
- Informed Consent signed by the subject.
- Single de novo target lesion stenosis of protected LMCA, or LAD, RCA or LCX (or of their branches) with\*:
- Stenosis of ≥70%;
- Stenosis ≥50% and \<70% (visually assessed) with evidence of ischemia via positive stress test, or fractional flow reserve value ≤0.80, or iFR \<0.90 or IVUS minimum lumen area ≤4.0 mm²;
- The target vessel reference diameter must be ≥2.5 mm \& ≤4.5mm;
- AND AT LEAST ONE OF THE FOLLOWING CRITERIA:
- Evidence of calcification at the lesion site by angiography (Grade 3), with fluoroscopic radio-opacities noted without cardiac motion prior to contrast injection involving both sides of the arterial wall in at least one location and total length of calcium of at least 15 mm and extending partially into the target lesion,
- AND/ OR by OCT, with presence of ≥270° calcium;
- AND/ OR Prior attempt at PCI with inability to expand a balloon in target lesion.
- Annotation: Only one lesion and vessel per randomized patient may be treated according to protocol and considered for the purpose of this study. The lesion considered for the study should represent the most calcified one.
Exclusion Criteria19
- Patient experienced an acute STEMI or cardiogenic shock related to an acute MI within 2 days prior to index procedure;
- Any comorbidity or condition which may reduce compliance with this protocol, including follow-up calls/ visits (e.g. advanced dementia);
- Any medical, geographic, and/or social factor making study participation impractical or precluding required follow-up.
- Patient is pregnant or nursing (a negative pregnancy test is required for women of child-bearing potential within 7 days prior to enrollment);
- Unable to take a P2Y12 inhibitor (i.e. clopidogrel, prasugrel, or ticagrelor) for at least 6 months;
- Patient has an allergy to imaging contrast media which cannot be adequately pre-medicated;
- Renal failure with an eGFR \<30ml/min1.73m2;
- History of a stroke or transient ischemic attack (TIA) within 7 days, or any prior intracranial hemorrhage;
- Active peptic ulcer or upper gastrointestinal (GI) bleeding within 6 months;
- Untreated pre-procedural hemoglobin \<10g/dL or intention to refuse blood transfusions if one should become necessary;
- Patient has an allergy or intolerance to cobalt-chromium and/ or everolimus.
- Life expectancy of less than 1 year.
- Anatomy where the device or OCT catheter are unlikely to be delivered due to tortuosity or other characteristics;
- Target lesion is in a coronary artery bypass graft;
- Target lesion is an in-stent restenosis (ISR);
- Flow limiting target vessel thrombus (evident on angiography or OCT);
- Definite or possible thrombus (by angiography or intravascular imaging) in the target vessel;
- Evidence of aneurysm in target vessel within 10 mm of the target lesion.
- Of note, only qualified physicians who are investigators or a sub-investigators for the trial will assess each individual´s eligibility criteria and take the final decision to include the subject in the trial (ICH GCP 4.3.1). This decision will be documented prior to the subject receiving the first intervention.
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Interventions
In order to permit advancement of the studied medical devices - OPN™ NCB or Shockwave™ IVL balloon catheter - initial lesion preparation using small SCBs or NCBs (≤2mm) or rotablation (Boston Scientific, Marlborough, MA, United States) is allowed, but will be documented. This may be required in selected cases with very calcified and tight lesions. As per protocol, lesion preparation will be performed using either the super-high pressure PCI balloon OPN™ NCB or the Shockwave™ IVL balloon catheter according to random treatment assignment after matching the angiographic and/or OCT inclusion criteria. Following successful lesion preparation all patients will be treated with a latest generation durable polymer everolimus-eluting stent (Xience™ Sierra or Skypoint, Abbott Vascular Inc., Santa Clara, CA, United States) to allow comparison of stent expansion.
In order to permit advancement of the studied medical devices - OPN™ NCB or Shockwave™ IVL balloon catheter - initial lesion preparation using small SCBs or NCBs (≤2mm) or rotablation (Boston Scientific, Marlborough, MA, United States) is allowed, but will be documented. This may be required in selected cases with very calcified and tight lesions. As per protocol, lesion preparation will be performed using either the super-high pressure PCI balloon OPN™ NCB or the Shockwave™ IVL balloon catheter according to random treatment assignment after matching the angiographic and/or OCT inclusion criteria. Following successful lesion preparation all patients will be treated with a latest generation durable polymer everolimus-eluting stent (Xience™ Sierra or Skypoint, Abbott Vascular Inc., Santa Clara, CA, United States) to allow comparison of stent expansion.
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT05346068