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NCT Number: NCT07382154

Target Vessel Failure After Laser Assisted Percutaneous Angioplasty Versus Balloon-based Treatment for Drug Eluting In-stent Restenosis

Stent restenosis (ISR) is an increasingly common problem; in fact, approximately 10% of coronary angioplasty procedures involve the treatment of a previously implanted stent. In cases of ISR of drug-eluting stents, the rate of further restenosis remains high (approximately 13% at one year). The treatment of stent restenosis consists of the use of balloon-based methods. Some small, single-center observational studies suggest the effectiveness of Excimer Laser Coronary Atherectomy (ELCA) in this context, allowing for a wider coronary lumen, a better minimum stent area (MSA), and a numerically lower incidence of new stent restenosis.

Demonstrating that Excimer Laser Coronary Atherectomy (ELCA)-assisted angioplasty treatment for DES ISR is associated with a lower incidence of Target Vessel Failure at 1 year compared to balloon-based angioplasty techniques may allow for better treatment of this type of patient.

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Key information

Conditions

Age range

19 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

About this study

Stent restenosis (ISR) is an increasingly common problem; in fact, approximately 10% of coronary angioplasty procedures involve the treatment of a previously implanted stent. ISR is defined as a 70% narrowing of the visually estimated coronary lumen within 5 mm of the proximal and distal portions of a previously implanted stent or, alternatively, a 50% narrowing associated with evidence of functional significance (e.g., ischemic symptoms or abnormal flow reserve). Treatment of ISR in bare-metal stents (BMS) has been shown to be safe and effective using both drug-eluting stents (DES) and drug-coated balloons (DCB). However, in the case of DES ISR, the rate of further restenosis is still high (approximately 13% at one year). The treatment of stent restenosis consists of the use of balloon-based methods, i.e., coronary balloons of various types, which may include the use of semi-compliant, non-compliant, scoring balloons, cutting balloons, with subsequent implantation of a new coronary stent or the elution of an antiproliferative drug with DCB. Some small observational monocentric studies suggest the efficacy of Excimer Laser Coronary Atherectomy (ELCA) in this context, allowing for a wider coronary lumen, a better minimum stent area (MSA), and a numerically lower incidence of new stent restenosis. One of the biases of these studies, in addition to the small sample size, is the type of contrast used to perform ELCA treatment. In fact, in a significant number of patients, saline solution was used, which is known to reduce the effectiveness of this therapy.

Recent registry studies show a one-year restenosis recurrence rate of approximately 5% in patients treated for ISR with ELCA without the use of saline solution. However, these studies are insufficient to clearly define whether ELCA can be considered the treatment of choice in this context, as they are too small to evaluate the effect on clinical outcomes or do not have a control group treated with traditional techniques. The ability of ELCA treatment to remove intrastent neo-atherosclerotic tissue and resolve the under-expansion of previously implanted coronary stents are the reasons why better results than conventional techniques are expected in DES ISR angioplasty. In fact, these two components are considered among the main causes of new restenosis. Therefore, an ad hoc study with adequate statistical power may be able to demonstrate a significant reduction in target vessel failure (TVR), i.e., an event related to the treatment of the vessel site of stent restenosis, one year later in patients with DES ISR thanks to ELCA treatment compared to balloon-based therapy.

Demonstrating that Excimer Laser Coronary Atherectomy (ELCA)-assisted angioplasty treatment for DES ISR is associated with a lower incidence of Target Vessel Failure at 1 year compared to balloon-based angioplasty techniques may allow for better treatment of this type of patient.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients aged ≥ 18 years who have undergone coronary angioplasty for restenosis of a drug-eluting stent in at least one coronary vessel
  • Acquisition of written informed consent from patients included in the study
  • 1-year follow-up in patients in the retrospective cohort

Exclusion criteria

  • concurrent presence of a new angiographically significant lesion on the coronary artery treated for ISR
  • hybrid treatment of two or more drug-eluting stent restenoses in the same angioplasty procedure. That is, treatment of one or more restenoses with balloon-based therapy alone and treatment of one or more restenoses using the ELCA technique in the same angioplasty procedure.
  • inability to take dual antiplatelet therapy for the period required by the coronary angioplasty procedure 4) life expectancy < 1 year

Treatment and study plan

Primary outcomes

  1. Number of "Target Vessel Failure" (TVF)

    Time frame: 1 year after the procedure

    The TVF number will be calculated by considering the number of patients who experienced at least one of the events that make up the primary TVF outcome (cardiac death due to heart attack, non-fatal myocardial infarction, clinically guided revascularization, angiographic restenosis) in the group treated with balloon-based techniques and in the group treated with ELCA.

Secondary outcomes

  1. Degree of stent expansion

    Time frame: During the procedure

    The degree of stent expansion will be assessed by measuring:

    • Minimum stent area on intracoronary imaging (MSA)
    • Stent expansion (SE)

Study contacts

Contact information is provided by the study sponsor or research team.

Gabriele Ghetti, MD

CONTACT

[email protected]

+39 0512144475

Sponsors and collaborators

Lead sponsor

IRCCS Azienda Ospedaliero-Universitaria di Bologna

Other

Registry information

Acronym: SONIC

Important dates

Study start
2026
Primary completion
2027
Study completion
2028
First posted
Feb 2, 2026
Registry last updated
Feb 2, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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