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临床试验/NCT07407738
NCT07407738招募中不适用

ShockFast Intravascular Lithotripsy Device for Treatment of Calcified Coronary Lesions, a Prospective, Randomised, International Trial: ShockFast IVL Trial

Shunmei Medical15 个研究点 分布在 4 个国家目标入组 120 人开始时间: 2026年2月16日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
120
试验地点
15
主要终点
Stent area post PCI measured at the minimal lumen area during initial procedure, evaluated by OCT

研究概览

简要总结

Coronary artery disease is caused by narrowing of the artery lumen. Treatment with Percutaneous Coronary Intervention (PCI) may be needed. This is a minimally invasive procedure used to treat narrowed or blocked coronary arteries. Sometimes a stent is placed to keep the artery open. If the lesions in the coronary artery are calcified, this may cause difficulties for successful stent placement. The calcified plaques can be fractured via intravascular lithotripsy (IVL) with devices like ShockWave IVL and ShockFast IVL. The aim of this study is to compare the this relatively new ShockFast IVl with the more widely used ShockWave IVL.

详细描述

Coronary calcified lesions have evolved as one of the most challenging indications for coronary percutaneous interventions (PCI). Different dedicated devices have been recently introduced into the market to improve procedural success in this challenging PCI population. Shockwave Intravascular Lithotripsy, (Shockwave IVL), Shockwave Medical, SC, CA, USA, was the first intracoronary device that used sonic pressure to fracture intracoronary calcium. The device safety and efficacy has been proved in a series of clinical trials. ShockFast intravascular lithotripsy (ShockFast IVL), Shunmei medical, Shenzhen, China, is a new dedicated device to treat intracoronary calcium that makes use of sonic pressure waves to fracture calcified plaques. ShockFast IVL has recently obtained CE mark approval for this indication.

The aim of this study is to compare this new lithotripsy device (ShockFast IVL) with the existing and widely used lithotripsy device that uses the same principle of action, the Shockwave IVL, Shockwave Medical, SC, CA, USA.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients aged ≥18 years undergoing PCI for stable or unstable angina or staged procedure after successful treatment of a myocardial infarction where heart enzymes are decreasing
  • Angiographic criteria:
  • Native de novo coronary lesions
  • Vessel diameter between 2.5mm - 4.0mm
  • Lesion Length: ≤40mm
  • Severe Calcification:
  • Calcification visible on the upper and the lower sides of the vessel wall in at least two angiographic projections that differ ≥ 60° from each other
  • Presence of severe calcified protruding noduli
  • No flow disturbances at baseline (Thrombolysis in Myocardial Infarction [TIMI] 3 flow at baseline)
  • Target lesion with diameter stenosis ≥70% by visual, or ≥50% with evidence of clinical ischemia
  • OCT Criteria:
  • Total calcium arc > 180° or
  • Presence of a protruding calcified noduli

排除标准

  • Ejection fraction less than 25%
  • Lesion located in Left Main (LM) coronary artery
  • Calcifications located mostly > 0.5 mm from the vessel lumen.
  • Severe renal Impairment; Serum Creatinine > 220 μmol or currently undergoing hemodialysis
  • Severe lesion tortuosity where OCT is judged impossible to cross.
  • Inability to tolerate dual antiplatelet therapy for 6 months or longer
  • Inability to obtain inform consent or deemed poorly compliant by the investigator
  • Presence of permanent pacemaker
  • Angiographic evidence of thrombus in the target vessel
  • Target lesion located at or involving within 5mm of the coronary ostium of the Left Anterior Descending artery (LAD), Left Circumflex artery (LCX)
  • Target lesion is a chronic total occlusion (CTO)
  • Presence of aneurysm within 10mm proximal or distal to the target lesion

研究组 & 干预措施

Shockfast IVL

Experimental

Interventional procedure using a dedicated device to treat coronary calcified lesions by offering precise control of sonic pressure waves for safe fracture calcium deposits within the artery walls, thus maintaining vessel flexibility and promoting smoother stent placement. The ShockFast device has an improved crossing profile and 2 lengths of the catheter: 12 and also 15mm compared to ShockWave which has only 1 length.

干预措施: Shockfast IVL (Device)

Shockwave IVL

Active Comparator

Interventional procedure that utilizes a fluid-filled catheter connected to an energy source that generates mechanistically tuned ultrasonic acoustic pressure waves - or Shockwaves - for modification, fracture, and fragmentation of vascular calcification.

干预措施: Shockwave IVL (Device)

结局指标

主要结局

Stent area post PCI measured at the minimal lumen area during initial procedure, evaluated by OCT

时间窗: Hospitalisation (during procedure)

次要结局

  • Target lesion failure defined as cardiac death, target-vessel myocardial infarction and target-lesion revascularisation at discharge and 30 days(30 day follow-up)
  • Angiographic success(Hospitalisation (during procedure))
  • Device success(Hospitalisation (during procedure))

研究者

发起方
Shunmei Medical
申办方类型
Industry
责任方
Sponsor

研究点 (15)

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