PET scans may reveal which aortic valves will worsen
NCT ID NCT07819344
First seen Sep 14, 2026 · Last updated Sep 17, 2026 · Updated 3 times
Summary
Researchers at Massachusetts General Hospital are studying whether molecular imaging and detailed biological profiling can predict how quickly aortic stenosis gets worse. The trial enrolls 100 adults with mild to moderate calcific aortic stenosis. Participants receive a baseline PET/CT scan to measure active calcification in the valve, and researchers use multi-omics data to build prediction models. Follow-up imaging after one year tracks changes in the valve to see if the baseline measures match the rate of progression.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- 18F-sodium fluoride PET/CT imaging
- What this could lead to
- If it works, this could give doctors a way to predict whose aortic stenosis will worsen quickly, helping them plan treatment earlier.
- What could go wrong
- The study is small and observational, so the prediction models may not hold up in larger or different groups. PET/CT also involves radiation exposure.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Mar 2031
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
100 subjects with mild or moderate aortic stenosis
- 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: * Males and females * aged 18 years or older * mild to moderate calcific Aortic Stenosis (as defined by standard echocardiographic criteria) Exclusion Criteria: * Bicuspid Aortic Stenosis * pregnancy * cognitive disabilities that impair the ability to comply with instructions or provide informed consent * any other medical condition that may undermine participation * weight \>300 lbs * severe claustrophobia * Pregnancy * subjects who have had significant radiation exposure as part of research (\>2 nuclear tests, computed tomography images, or fluoroscopic procedures) during the preceding 12 months * Individuals with renal dysfunction (eGFR\<55) or a history of allergic reaction to iodinated contrast will not receive the iodinated contrast.
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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 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.
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