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Rationale and design of a study exploring the efficacy of once-daily oral rivaroxaban (X-TRA) on the outcome of left atrial/left atrial appendage thrombus in nonvalvular atrial fibrillation or atrial flutter and a retrospective observational registry providing baseline data (CLOT-AF)

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dc.contributor.author Lip, Gregory-Y-H
dc.contributor.author Hammerstingl, Christoph
dc.contributor.author Marín, Francisco
dc.contributor.author Cappato, Riccardo
dc.contributor.author Meng, Isabelle-Ling
dc.contributor.author van-Eickels, Martin
dc.contributor.author Kirsch, Bodo
dc.contributor.author Morandi, Eolo
dc.contributor.author Cohen, Ariel
dc.date.accessioned 2026-10-21T06:10:13Z
dc.date.available 2026-10-21T06:10:13Z
dc.date.issued 2015-04
dc.identifier.citation Lip GYH, Hammerstingl C, Marin F, Cappato R, Meng IL, Kirsch B, et al. Rationale and design of a study exploring the efficacy of once-daily oral rivaroxaban (X-TRA) on the outcome of left atrial/left atrial appendage thrombus in nonvalvular atrial fibrillation or atrial flutter and a retrospective observational registry providing baseline data (CLOT-AF). American Heart Journal. abril de 2015;169(4):464-471.e2. doi:10.1016/j.ahj.2014.12.020
dc.identifier.issn 0002-8703
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/28709
dc.description.abstract There are still many unresolved issues concerning patient outcomes and prognostic factors in patients with atrial fibrillation (AF) and left atrial/left atrial appendage (LA/LAA) thrombi. Rivaroxaban (Xarelto®), a potent and highly selective oral, direct factor Xa inhibitor, is a new therapeutic option in this setting. The planned study program will consist of a prospective interventional study (X-TRA) and a retrospective observational registry (CLOT-AF). The primary objective of the X-TRA study is to explore the efficacy of rivaroxaban in the treatment of LA/LAA thrombi in patients with nonvalvular AF or atrial flutter, scheduled to undergo cardioversion or AF ablation, in whom an LA/LAA thrombus has been found on transesophageal echocardiography (TEE) before the procedure. The primary end point is the complete LA/LAA thrombus resolution rate at 6 weeks of end of treatment confirmed by TEE. The secondary objectives are to describe categories of thrombus outcome in patients (resolved, reduced, unchanged, larger, or new) confirmed on TEE at the end of treatment (after 6 weeks of treatment), incidence of the composite of stroke and noncentral nervous system systemic embolism at the end of treatment and during follow-up, and incidence of all bleeding at the end of treatment and during follow-up. The objective of the CLOT-AF registry is to provide retrospective thrombus-related patient outcome data after standard-of-care anticoagulant treatment in patients with nonvalvular AF or atrial flutter, who have TEE-documented LA/LAA thrombi. The data will be used as a reference for the prospective X-TRA study. In conclusion, X-TRA and CLOT-AF will provide some answers to the many unresolved issues concerning patient outcomes and prognostic factors in patients with AF and LAA thrombi. Results from this study program would provide the first prospective interventional study (X-TRA) and a large international retrospective observational registry (CLOT-AF) on the prevalence and natural history of LA/LAA thrombi. Unique data on clot resolution with rivaroxaban in a prospective cohort would be obtained in X-TRA.
dc.language.iso eng
dc.rights Atribución/Reconocimiento-NoComercial-SinDerivados 4.0 Internaciona
dc.rights.uri https://creativecommons.org/licenses/by-nc-nd/4.0/deed.es *
dc.subject.mesh Female
dc.subject.mesh Humans
dc.subject.mesh Male
dc.subject.mesh Middle Aged
dc.subject.mesh Administration, Oral
dc.subject.mesh Atrial Appendage
dc.subject.mesh Atrial Fibrillation/complications/diagnosis/therapy
dc.subject.mesh Catheter Ablation
dc.subject.mesh Dose-Response Relationship, Drug
dc.subject.mesh Drug Administration Schedule
dc.subject.mesh Echocardiography, Transesophageal
dc.subject.mesh Electric Countershock
dc.subject.mesh Factor Xa Inhibitors/administration & dosage
dc.subject.mesh Heart Diseases/diagnostic imaging/drug therapy/etiology
dc.subject.mesh Morpholines/administration & dosage
dc.subject.mesh Retrospective Studies
dc.subject.mesh Rivaroxaban
dc.subject.mesh Thiophenes/administration & dosage
dc.subject.mesh Thrombosis/diagnostic imaging/drug therapy/etiology
dc.subject.mesh Treatment Outcome
dc.subject.mesh Randomized Controlled Trials as Topic
dc.subject.mesh Multicenter Studies as Topic
dc.subject.mesh Observational Studies as Topic
dc.title Rationale and design of a study exploring the efficacy of once-daily oral rivaroxaban (X-TRA) on the outcome of left atrial/left atrial appendage thrombus in nonvalvular atrial fibrillation or atrial flutter and a retrospective observational registry providing baseline data (CLOT-AF)
dc.type info:eu-repo/semantics/article 
dc.identifier.pmid 25819852
dc.relation.publisherversion https://linkinghub.elsevier.com/retrieve/pii/S0002870315000113
dc.type.version info:eu-repo/semantics/publishedVersion
dc.identifier.doi 10.1016/j.ahj.2014.12.020
dc.journal.title American Heart Journal
dc.identifier.essn 1097-5330


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