Biosense Webster, Inc. Launches US Clinical Study to Evaluate the Safety and Efficacy of the WaveCrest® Left Atrial Appendage Occlusion System to reduce stroke risk in atrial fibrillation patients.
Johnson & Johnson Medical Devices Companies announced that Biosense Webster, Inc., a worldwide leader in the diagnosis and treatment of heart arrhythmias, enrolled the first patient in the WaveCrest® Investigational Device Exemption (IDE) Trial.
The study will evaluate the safety and effectiveness of the WaveCrest® Left Atrial Appendage Occlusion (LAAO) System in closure of the Left Atrial Appendage (LAA) and evaluate the reduction of embolic stroke in atrial fibrillation (AFib) patients who cannot tolerate chronic Oral Anticoagulation Therapy (OAC).
The first patient was treated last week at New York University (NYU) Hospital by Larry Chinitz, a cardiac electrophysiologist, and director of NYU Langone’s Heart Rhythm Center in New York City. The trial will enroll 1,250 patients at approximately 90 hospitals, and follow them for five years.
“The WaveCrest® System is designed to enable physicians to close the heart’s LAA, where most stroke-causing blood clots occur,” said Dr. Chinitz. “For patients with AFib seeking an alternative to anticoagulants or blood thinners, this may be an important procedural option that could reduce the risk of stroke and save lives.”
According to the American Stroke Association, people with AFib have five times higher risk of stroke than the general population. The Centers for Disease Control and Prevention (CDC) estimates 87% of all strokes are ischemic strokes, in which blood flow to the brain is blocked by the formation of a clot.
“Preventing and reducing the risk of stroke in AFib patients is a significant unmet need,” said Shlomi Nachman, Company Group Chairman of Johnson & Johnson Medical Devices Cardiovascular & Specialty Solutions.
The study is a prospective, multicenter, randomized, active-controlled clinical trial of the WaveCrest® Left Atrial Appendage Occlusion System compared to an existing FDA-approved LAA Closure Device for the reduction in risk of embolic stroke in subjects with non-valvular atrial fibrillation.
Although the device is under clinical study and not approved for use in the US, the WaveCrest® Device is CE Mark approved and available in Europe.