Ultrasound may predict Stroke-Causing plaques
NCT ID NCT05218421
First seen Aug 19, 2026 · Last updated Aug 20, 2026 · Updated 1 time
Summary
This study is testing whether an advanced ultrasound technique can identify which carotid artery plaques are dangerous (vulnerable) and likely to cause a stroke. Researchers will compare ultrasound images taken before surgery with the actual plaque tissue removed during the operation. The goal is to see if this non-invasive imaging can reliably predict plaque risk, potentially helping doctors make better treatment decisions in the future.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Carotid ultrasound with flow and elastography measurements, plus blood and plaque analysis
- What this could lead to
- If successful, this could lead to a non-invasive way to identify high-risk carotid plaques before they cause strokes, guiding better treatment decisions.
- What could go wrong
- This is an observational study, so it won't test a treatment. The ultrasound technique may not accurately predict plaque vulnerability, and results may not apply to all patients.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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70 people
The number who actually took part.
- Started
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May 2022
- Finished
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Dec 2025
- 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.
Who is studied
Patients with a carotid artery stenosis ≥50% according to clinically performed imaging (i.e. duplex, computed tomography angiography (CTA), or magnetic resonance angiography (MRA)) that are scheduled for a CEA.
- Ages
-
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: * Presence of carotid artery stenosis (≥50%) according to conventional clinically performed imaging (duplex/CT(A)/MR(A)) and scheduled for a CEA; * Possibility to perform carotid ultrasound ≤2 weeks before the CEA * ≥18 years old; * Able to provide signed or oral informed consent. Exclusion Criteria: * Hampered carotid blood flow imaging during clinically performed duplex/doppler measurements due to near to total carotid occlusion at the side of interest or a calcified plaque; * Restenosis after carotid revascularisation at side of interest; * Participating in another clinical study, interfering on outcomes;
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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.
Contacts and locations
Locations
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Radboud university medical center
Nijmegen, Netherlands
-
Rijnstate Hospital
Arnhem, Netherlands
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- New monitoring technique for vascular surgery falls short