Common blood thinners may speed up artery calcification, study suggests
NCT ID NCT02823093
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether vitamin K antagonists (a type of blood thinner) are linked to more calcium buildup in the aorta, the body's main artery. Researchers compared 73 patients—some on the drug for at least 6 months and some who never took it—using CT scans. The goal was to see if these medications might contribute to artery hardening.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- vitamin K antagonists (blood thinners)
- What this could lead to
- If it succeeds, this could clarify whether vitamin K antagonists worsen aortic calcification, guiding safer prescribing.
- What could go wrong
- This is a small, observational study with only 73 participants, so results may not apply broadly. It cannot prove cause and effect.
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
-
73 people
The number who actually took part.
- Started
-
Apr 2016
- Finished
-
Mar 2021
- Lead sponsor
-
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
One group treated by VKA treatment for at least 6 months and one focus droup which have never been treated by VKA treatment.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
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: * patients having a abdominal scanner without injection planned at CHU Amiens * group treated by VKA: VKA treatment for at least 6 months * group not treated by VKA: no antecedent of AVK treatment Exclusion Criteria: * abdominal scanner contre indication * progressive cancer * scanner planned by emergency department * patient having had acute cardiovascular accident in the last 3 months
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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
-
CHU Amiens
Amiens, 80054, France
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Other studies related to the condition(s) this trial covers.
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