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Shockwave IVL + DCB

Intravascular Lithotripsy Plus Drug-coated Balloon in Calcified Small Coronary Vessels: a Feasibility Exploratory Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05625997
Enrollment
50
Registered
2022-11-23
Start date
2023-06-16
Completion date
2026-06-30
Last updated
2025-05-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Calcified Lesions in Small Coronary Vessels

Brief summary

Drug-eluting stent (DES) implantation as interventional strategy for lesions in small coronary arteries is the current standard of care in many centers worldwide, but is associated with increased risk of late treatment failure in small vessels, as compared with larger coronary arteries. Randomized and observational studies have been shown that coronary intervention with drug-coated balloons (DCB) provide a promising alternative to DES implantation in small vessels, while avoiding the risk of a permanent vascular implant. Furthermore, lesions in small vessels are frequently concomitant with diffuse disease and/or distal location, where the presence of calcification is an additional common feature. Intravascular lithotripsy (IVL) has been recently introduced as a novel adjunctive technology to treat calcified lesions. This study will explore the hypothesis that IVL has the potential to enhance the results of coronary balloon dilatation of small vessels with calcified lesions, therefore increasing the likelihood of optimal DBC intervention.

Interventions

None listed

Sponsors

Rede Optimus Hospitalar SA
Lead SponsorNETWORK

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Age 18 years or older 2. Coronary artery disease with percutaneous intervention clinically indicated to treat one or more lesions fulfilling all criteria below: * De novo lesion with diameter stenosis \> 50% (visual analysis) * Coronary vessel diameter \< 3.0 mm (visual analysis) * Severe calcification at the target segment, defined as fluoroscopic radiopacities noted without cardiac motion prior to contrast injection involving both sides of the arterial wall in at least 1 location OR Intravascular Ultrasound/Optical Coherence Tomography (IVUS/OCT) demonstrated calcium angle of ≥270° on at least 1 cross section. 3. Written informed consent

Exclusion criteria

1. Previous coronary intervention at or \< 10 mm distant from target segment at any time. 2. Lesion length ≥ 40 mm. 3. Planned atherectomy or cutting/scoring balloon use. 4. Bifurcation lesion. 5. Thrombus containing lesion. 6. Life expectancy \< 12 months due to other co-morbid condition(s) that could limit patient's ability to participate in clinical study

Design outcomes

Primary

MeasureTime frameDescription
Successful IVL plus DCBat 1 month follow-upSuccessful IVL plus DCB in the absence of target lesion failure (TLF); Successful IVL plus DCB will be defined as a composite of: * IVL application at the target site, AND * DCB inflation at the target site, AND * Residual in-segment diameter stenosis \<40% by quantitative coronary angiography, in the absence of final serious angiographic complications (≥ Grade D dissection, perforation, abrupt closure, final TIMI flow ≤ II), AND * Without the need for bailout scoring/cutting balloon or atherectomy-based strategy, AND * Without the need for bailout stenting. TLF will be defined as a composite of clinically driven revascularization, OR myocardial infarction, OR cardiac death related to the target lesion.

Countries

Brazil, Italy

Contacts

Primary ContactAnnelena Held-Wehmöller, PhD
shockwave_dcb@redeoptimus.com+4915785128140

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026