Blood thinners may dissolve clots on replacement heart valves, study hopes
NCT ID NCT02318342
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study will use advanced imaging to check for blood clots or other problems in 3000 people with artificial aortic heart valves. Those found to have clots will receive the blood thinner warfarin for three months, then be re-imaged to see if the clots have resolved. The goal is to determine if anticoagulation can effectively treat early valve dysfunction without the need for another surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Warfarin (also known as Coumadin)
- What this could lead to
- If successful, this could confirm that warfarin effectively dissolves early blood clots on artificial heart valves, improving valve function without surgery.
- What could go wrong
- This is an observational study with a treatment component, not a randomized controlled trial. Warfarin carries a risk of bleeding, and the study may not prove long-term benefits.
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.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 3,000 people
The number the study aims to enrol. It can still change while the study runs.
- Start date
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Dec 2014
- Expected to finish
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Dec 2028
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.
- 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.
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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 transcatheter or surgical bioprosthetic aortic valve implanted at least 48 hours prior to enrollment * Age 18 years or older * Ability to provide informed consent and follow-up with protocol procedures. Exclusion Criteria: * Renal insufficiency (creatinine \> 1.5 mg/dL) * Known allergy to iodinated contrast agents
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Get notified about this study
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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 places running it
1 site. The list below names each one and where it is.
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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.
Contacts and locations
Locations
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Cedars-Sinai Medical Center
RECRUITINGLos Angeles, California, 90048, United States