Shockwave therapy may improve stent success in hardened leg arteries
NCT ID NCT06112171
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether using a special shockwave device to break up calcium before placing a stent works better than the usual balloon angioplasty in people with peripheral artery disease (PAD) and heavily calcified leg arteries. About 120 participants will be randomly assigned to one of the two approaches. The goal is to see which method leads to better blood flow and fewer complications after stent placement.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 120 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2024
- Expected to finish
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Dec 2032
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Subject age ≥ 18 * Subject has been informed of the nature of the study, agrees to participate, and has signed a Medical Ethics Committee approved inform consent form * Subject understands the duration of the study, agrees to attend follow-up visits, and agrees to complete the required testing * Rutherford Classification 2-5 * Subject has a de novo or restenotic lesion in SFA and/or PPA not exceeding the medial femoral epicondyle with ≥ 70% stenosis documented angiographically * No previous stent in the target lesion, if target vessel was previously stented the stent should be at least 3cm apart * Target lesion length is ≥ 10cm, no maximum lesion length limit * Severe calcification on fluoroscopy defined by PACSS Grade 4: 1) bilateral calcification and 2) extending ≥50mm in length * Multiple lesions with max. 3cm healthy vessel segment in between lesions can be considered at the discretion of the operator as one lesion * Reference vessel diameter (RVD) ≥ 4 mm and ≤ 6.5 mm by visual estimation * Patency of at least one infrapopliteal artery to the ankle (\< 50% diameter stenosis) in continuity with the native femoropopliteal artery * A guidewire has successfully traversed the target treatment segment (both intraluminal and subintimal crossing allowed) Exclusion Criteria: * Failure to successfully cross the target lesion * Presence of fresh thrombus in the lesion * Presence of aneurysm in the target vessel/s * Presence of a stent in the target lesion, at least 3cm from any previously stent in target vessel * Prior vascular surgery of the target lesion * Stroke or heart attack within 3 months prior to enrollment * Enrolled in another investigational drug, device or biologic study that has not reached the primary endpoint * Life expectancy of less than one year * Known allergies or sensitivity to heparin, aspirin, other anticoagulant/ antiplatelet therapies or contrast media that cannot be adequately pre-treated prior to index procedure * Rutherford Classification of 0, 1, or 6 * Significant gastrointestinal bleeding or any coagulopathy that would contraindicate the use of anti-platelet therapy * Receiving immunosuppressant therapy * Pregnant or breast-feeding females * History of major amputation (defined as amputation above ankle joint) in the same limb as the target lesion
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University Clinic Leipzig
RECRUITINGLeipzig, Saxony, 04103, Germany
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