Rivaroxaban Evaluation in Real Life Settings

Thrombosis Research Institute5,278 enrolled

Overview

To discover outcomes of patients treated with Rivaroxaban with atrial fibrillation with at least one additional investigator-determined risk factor for stroke in real-life practice.

This large global registry focuses on studying Atrial Fibrillation (AF) and evaluating characteristics, management and outcomes of patients treated with Rivaroxaban. The RIVER registry is observational, decisions on patient management are determined by the health care professional and the patient and not by the protocol. Patients are therefore treated according to normal local practice and the drug label/relevant product information of any drugs administered to them.

Study Type

OBSERVATIONAL

Enrollment

5,278

Conditions

Atrial Fibrillation Stroke

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Written informed consent * Age 18 years and over * New diagnosis of non-valvular atrial fibrillation (diagnosed within the last 6 weeks) with at least one additional investigator-determined risk factor for stroke * Initial treatment with Rivaroxaban following AF diagnosis Exclusion Criteria: * No further follow-up envisaged or possible within enrolling hospital or with associated primary care physician. * Patients with transient AF secondary to a reversible cause. * Patients participating in an interventional study that dictates treatments, visit frequency or diagnostic procedures * Not treated with Rivaroxaban as first treatment

Locations (2)

Prof. Jean-Yues LeHeuzey, National Coordinating Investigator, Hopital Europeen Georges Pompidou

Paris, France

Thrombosis Research Institute

London, United Kingdom

Outcomes

Primary Outcomes

Rate of Stroke in Registry participants

To assess the rate of stroke and systemic embolisation in registry participants

Time frame: 2 years

Rate of Systemic Embolisation in Registry participants

To assess the rate of stroke and systemic embolisation in registry participants

Time frame: 2 years

Data from ClinicalTrials.gov

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