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Anticoagulation Therapy in Non-device-related Intra-cardiac Thrombus
Sponsor: Centre Hospitalier Universitaire de Nīmes
Summary
Left ventricular thrombus is found in 10 to 25% of patients with impaired left ventricular function following ST-segment elevation myocardial infarction and up to 20% in dilated cardiomyopathy in observational studies. Likewise, the incidence of atrial thrombus among atrial fibrillation patients treated by vitamin K antagonist (VKA) is between 0.25% and 7%. Despite anticoagulant therapy, intra-cardiac thrombus remains a severe complication associated with a high risk of systemic embolism and subsequent mortality but also bleeding events related to the anticoagulation therapy. The class of non-vitamin K antagonist direct oral anticoagulant (DOA) has emerged in the last decades and has systematically surpassed VKA in the different clinical settings by providing at minimum a similar efficacy and a better safety profile. In the absence of randomized study in the specific clinical setting of intracardiac thrombus, international Guidelines recommend, on the basis of expert opinion, the use of VKA for at least 3 to 6 months in case of left ventricular thrombus and there is no specific recommendation for thrombus management from other cardiac localizations. In comparison to VKA, the easier management and the large evidence of better safety of DOA make it an interesting anticoagulant strategy. Data for left ventricule thrombosis treatment are limited and only supported by observational cohorts. However, these recent cohorts have shown promising data in this indication reporting similar thrombus regression following DOA in comparison to VKA and similar ischemic outcomes although no head-to-head comparison would be powered. As a consequence, the multicentric randomized ARGONAUT trial aims to confirm these results and evaluate the impact of DOA compared to VKA on thrombus regression and clinical outcomes among patients with intracardiac thrombus, regardless of the thrombus localization and any underlying heart disease.
Official title: Anticoagulant Regimens Given to Achieve Thrombus Regression and Reduce Clinical Outcomes Among Patients With Non Device-related Intra-cardiac Thrombus: a Randomized Assessment Under Direct Oral Anticoagulant and Vitamin-k Antagonist Therapy
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
340
Start Date
2023-05-15
Completion Date
2026-02
Last Updated
2026-02-17
Healthy Volunteers
No
Conditions
Interventions
Vitamin K antagonist
VKA study medications (Warfarin, Fluindione and Acenocoumarol) will be prescribed and supplied in the usual setting of patient care with respect of the international guidelines and recommended dose protocols and will not be specifically supplied for the trial. Anticoagulant treatment will be prescribed for 6 months. The recommended INR target will be \[2-3\] and \[2-2.5\] for patients treated with concomitant antiplatelet therapy. Biological monitoring will be performed at discretion of physicians as usual care.
Direct oral anticoagulant
DOA study medications (Apixaban, Rivaroxaban and Dabigatran) will be prescribed and supplied in the usual setting of patient care and will not be specifically supplied for the trial. The usual doses of DOA will be prescribed: dabigatran 150mg twice a day, apixaban 5mg twice a day and rivaroxaban 20mg once a day. The adjusted doses (dabigatran 110mg twice a day, apixaban 2.5mg twice a day and rivaroxaban 15mg once a day) will be prescribed according to clinical practice treatment guidelines.
Locations (35)
CHU Angers
Angers, France
Ch Auxerre
Auxerre, France
Ch Avignon
Avignon, France
CH Bastia
Bastia, France
Hôpital Cardiologique du Haut Lévêque
Bordeaux, France
CHU Brest
Brest, France
CH Chartres
Chartres, France
CHU Gabriel Montpied
Clermont-Ferrand, France
CH Compiègne Noyon
Compiègne, France
Hôpital Privé Dijon Bourgogne
Dijon, France
Groupe Hospitalier Mutualiste
Grenoble, France
CHU Lille
Lille, France
CHU Limoges
Limoges, France
Hôpital Cardiovasculaire Louis Pradel
Lyon, France
AP-HM CHU La Timone
Marseille, France
CHR Metz-Thionville
Metz, France
CHU Arnaud de Villeneuve
Montpellier, France
Clinique du Millenaire
Montpellier, France
CHU Nantes
Nantes, France
CHU Nice
Nice, France
CHU de Nimes
Nîmes, France
AP-HP CHU Bichat
Paris, France
AP-HP CHU Lariboisière
Paris, France
Ap-Hp Hegp
Paris, France
AP-HP Hopital Ambroise Paré
Paris, France
CHU Pitié-Salpêtrière
Paris, France
CH Francois Mitterand
Pau, France
CHU Poitiers
Potiers, France
CHU Rennes
Rennes, France
Centre Cardiologique du Nord
Saint-Denis, France
CHU Strasbourg
Strasbourg, France
CHU Toulouse
Toulouse, France
Centre Hopistalier de Valence
Valence, France
Ch Bretagne Atlantique
Vannes, France
CHU La réunion NORD
Saint-Denis, Reunion