Microplastics in your blood: a hidden heart risk?
NCT ID NCT07748767
First seen Aug 06, 2026 · Last updated Aug 21, 2026 · Updated 2 times
Summary
This study looks at whether tiny plastic particles in the blood are linked to problems with the heart's small blood vessels. Researchers will measure microplastic levels in 184 people who are already having a heart procedure, and then check their heart vessel function and track their health for two years. The goal is to see if higher plastic exposure is associated with worse heart outcomes.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- micro-nanoplastic examination (blood test for microplastics)
- What this could lead to
- If microplastics are found to harm heart blood vessels, this could lead to new ways to prevent or treat heart disease by reducing plastic exposure.
- What could go wrong
- This is an observational study, so it can only show a link, not prove cause and effect. The results may be affected by other factors, and the study is relatively small.
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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About 184 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jan 2027
An estimate. Start dates often move.
- Expected to finish
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Dec 2029
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 older than 18 years old, with clinical indications for planned invasive coronary angiography and coronary functional assessment.
- 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: * Age ≥ 18; * Patients with clinical indications for undergoing invasive coronary angiography and coronary functional assessment (including fractional flow reserve \[FFR\], CFR, and IMR); * Voluntarily sign the written informed consent form. Exclusion Criteria: * The surgeon (or attending physician) determines that the patient is not suitable for or cannot tolerate a coronary physiological examination; * Intraoperative coronary angiography reveals a stenosis of\>90% in any non-left main coronary artery lumen or a stenosis of\>50% in the left main coronary artery lumen; * Left ventricular ejection fraction \<35% or cardiogenic shock or cardiac arrest; * Previous history of invasive procedures/treatments; * Active inflammatory diseases; * Connective tissue disease; * History of malignant tumors; * Expected lifespan \<2 years; * Pregnancy or lactation; * Subjects who refuse to comply with the pollution control measures set in this study; * Currently participating in other interventional clinical trials.
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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
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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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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Other studies related to the condition(s) this trial covers.
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