AzTrials
AzTrials

In-stent RestenosisSONICNCT07382154

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

An observational study of In-stent Restenosis, run by IRCCS Azienda Ospedaliero-Universitaria di Bologna at 1 site in Italy.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
Search all trials

Trial summary

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). Read more about this study

Who is it for?
Ages 19 years and older
Conditions the study is for
In-stent Restenosis
How many people
1,260 participants
Where
1 siteItaly
Study dates
Feb 2026to Jul 2028
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 19 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: The study plans to enroll patients aged ≥ 18 years who have undergone coronary angioplasty for DES restenosis. It will be a retrospective and prospective multicenter national cohort study.

Who may be able to join

  • 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

Who cannot join

  • 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

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Gabriele Ghetti, MD contact

+39 0512144475

gabriele.ghetti@aosp.bo.it

Italy1 site
  • IRCCS Policlinico di Sant'Orsola

    Bologna, 40138

    Gabriele Ghetti, MD, +39 0512144475, gabriele.ghetti@aosp.bo.it

Other trials in Italy

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. 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.

Read the detailed description

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.

Keywords
in-stent restenosis, drug-eluting stents, Excimer Laser Coronary Atherectomy

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07382154
Study groupRoleWhat they receive
patients aged ≥ 18 years who have undergone coronary angioplasty for DES restenosisNot described

What is being measured

The primary outcome is the main question the study is designed to answer.

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

    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.

    Measured: 1 year after the procedure

Secondary outcomes (1)
  1. Degree of stent expansion

    The degree of stent expansion will be assessed by measuring:

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

    Measured: During the procedure

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Feb 2026
  2. Study startFeb 2026 (estimated)
  3. Primary completionOct 2027 (estimated)
  4. Study completionJul 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Other
Enrolment
1,260 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07382154
Sponsor's protocol ID
SONIC
Acronym
SONIC
Status last verified
Jan 2026
First submitted
26 Jan 2026
Last updated
2 Feb 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of In-stent Restenosis, run by IRCCS Azienda Ospedaliero-Universitaria di Bologna at 1 site in Italy.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 2 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Gabriele Ghetti, MD (+39 0512144475, gabriele.ghetti@aosp.bo.it), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of "Target Vessel Failure" (TVF) (time frame: 1 year after the procedure). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Feb 2026.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in