Intravascular Lithotripsy Versus Conventional Therapy for Severely Calcified Coronary Artery Lesions (NCT06238518) | Clinical Trial Compass
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Intravascular Lithotripsy Versus Conventional Therapy for Severely Calcified Coronary Artery Lesions
China220 participantsStarted 2024-01-05
Plain-language summary
Percutaneous coronary intervention (PCI) encounters challenges with calcified coronary lesions, leading to potential issues such as failed balloon dilatation, incomplete stent expansion, and increased risks of adverse events post-PCI, including stent restenosis and thrombosis.
Intravascular lithotripsy (IVL), a novel approach for severely calcified coronary lesion preparation, has shown promising preliminary outcomes. Combining IVL with conventional approaches, such as Rotational atherectomy (RA), non-compliant balloons, or cutting balloons, may associated with additional benefit than conventional approaches only in terms of better stent expansion and lower long-term adverse events.
This pilot randomized trial aims to investigate whether combining IVL to conventional therapy surpasses the efficacy of conventional approaches alone. The primary effectiveness endpoint is final stent expansion assessed by post-procedure optical coherence tomography (OCT), and the primary safety endpoint is target lesion failure (TVF). The trial seeks to provide valuable insights into the optimal approach for managing severely calcified coronary lesions during PCI.
Who can participate
Age range18 Years
SexALL
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Inclusion criteria
✓. Patients with acute or chronic coronary artery syndrome indicated for PCI with stenting.
✓. Able to understand and provide informed consent and comply with all study procedures
✓. Native and de novo coronary artery disease
✓. Lesion navigable by a 0.014" guidewire.
✓. Target lesion is severely calcified, meeting one of the following criteria:
Exclusion criteria
✕. Patients under 18 years of age.
✕. Incapable of providing informed consent.
✕. Female patients who are pregnant or nursing (a pregnancy test must be conducted within 7 days before the index procedure for women of childbearing potential, as per local practice).
✕. Concurrent medical conditions with a life expectancy of less than 1 year.
✕. Hemodynamic instability.
What they're measuring
1
Final stent expansion (%) assessed by OCT
Timeframe: Measured by the data collected at the end of the PCI procedure