Heart clot showdown: could a simpler blood thinner replace warfarin?
NCT ID NCT07709780
First seen Jul 17, 2026 · Last updated Jul 17, 2026
Summary
This trial tests whether apixaban, a newer blood thinner with fixed dosing, works as well as warfarin for dissolving dangerous blood clots in the heart's main pumping chamber. Adults with a confirmed left ventricular thrombus are randomly assigned to receive either apixaban or warfarin for at least three months. The main goal is to see if apixaban is no worse than warfarin at completely clearing the clot, as seen on heart MRI scans.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- apixaban and warfarin
- What this could lead to
- If apixaban works as well as warfarin, it could offer a simpler, safer treatment option for left ventricular thrombus without the need for frequent blood monitoring.
- What could go wrong
- This is a relatively small trial, and apixaban may not prove as effective as warfarin for dissolving the clot. Bleeding risks exist with both drugs.
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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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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About 218 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jun 2026
An estimate. Start dates often move.
- Expected to finish
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Jul 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.
- 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 years * LV thrombus confirmed within 14 days prior to randomization by CMR or contrast TTE or cardiac CT; baseline CMR required pre-randomization (or ≤7 days post-randomization if clinically unavoidable) * Candidate for oral anticoagulation for ≥3 months * Able to provide informed consent. Exclusion Criteria: * Absolute indication for VKA (mechanical valve, moderate-severe rheumatic MS and antiphospholipid syndrome) or clear preference or contraindication for one of the study drugs precluding randomization (see below) * Antiphospholipid syndrome * Estimated CrCl \<15 mL/min or dialysis * Severe hepatic impairment (ICD-10: K70.40, K70.41, K71.10, K71.11, K72.00, K72.01, K72.10, K72.11, K72.90, K72.91) * Active clinically significant bleeding * Platelets \<50,000/µL * Pregnancy or lactation; women of childbearing potential unwilling to use contraception * Life expectancy \<1 year or other conditions compromising follow-up Additional contraindications to use of warfarin or apixaban. This includes, but is not limited to: * Active pathological bleeding, major bleeding diathesis, or known blood dyscrasia * Recent or planned surgery involving the central nervous system or eye, traumatic surgery with large open surfaces, or procedures (spinal/epidural puncture or major regional block anesthesia) where bleeding cannot be safely controlled. * Conditions associated with high risk of bleeding such as threatened abortion, eclampsia, severe preeclampsia, or malignant/uncontrolled hypertension. * History of severe hypersensitivity or allergy to warfarin or apixaban. * Ongoing treatment with a combined P-gp and strong CYP3A4 inhibitor or inducer that cannot be safely discontinued or substituted. Examples include strong combined inhibitors such as ketoconazole, itraconazole, ritonavir or posiconazole, and strong combined inducers such as rifampin, carbamazepine, phenytoin, and St. John's wort.
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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 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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Banner University Medical Center - Tucson
RECRUITINGTucson, Arizona, 85724, United States
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