3D ultrasound could spot hidden clot risks in aneurysms
NCT ID NCT05841524
First seen Jul 21, 2026 · Last updated Jul 22, 2026 · Updated 1 time
Summary
This study explores whether a special 3D ultrasound technique, called vector flow imaging, can predict where blood clots form inside abdominal aortic aneurysms. Researchers will scan 14 people with small aneurysms (under 5.5 cm), half with existing clots and half without. They will also test whether injecting contrast microbubbles improves the image quality. The goal is to see if this non-invasive method can reliably measure blood flow patterns linked to clot formation.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this imaging technique could help predict which aneurysms are at risk of forming dangerous blood clots, guiding earlier treatment.
- What could go wrong
- This is a very small feasibility study with only 14 participants, so results may not apply broadly. The technique is still experimental and not ready for routine use.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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14 people
The number who actually took part.
- Started
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Apr 2023
- Expected to finish
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Dec 2026
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.
Who is studied
Patients diagnosed with an AAA. Both with and without intraluminal thrombus present.
- 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: * Diagnosed with AAA * AAA diameter below treatment threshold of 5.5 cm Exclusion Criteria: * Hypersensitivity to the active substance(s) or any of the excipients in Sonovue * Right-to-left cardiac shunt * Severe pulmonary hypertension (pulmonary artery pressure \> 90mmHg) * Uncontrolled systemic hypertension * Severe pulmonary disease (e.g. COPD GOLD 3 or 4, adult respiratory distress syndrome) * Clinically unstable cardiac disease (recent, \< 3 months, or ongoing myocardial infarction, unstable angina at rest, recent percutaneous coronary intervention, clinically worsening cardiac symptoms, severe cardiac arrhythmia's, endocarditis, etc.) * Prosthetic valves * Loss of renal function (GFR \< 31 ml/min), end-stage renal disease * End-stage liver disease * Sepsis
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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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St. Olavs hospital, Trondheim University Hospital
Trondheim, Trøndelag, 3250, Norway
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Other studies related to the condition(s) this trial covers.
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