Trial Number

415-23

Condition

Heart Failure

Participant Age Range

40 years and older

Participant Gender

Any

Enrolling Participants

Yes

Overview

Safety and Efficacy of the Alleviant System for No-Implant Interatrial Shunt Creation in Patients with Chronic Heart Failure

This purpose of this study is to evaluate the safety and efficacy of a percutaneously created interatrial shunt using the Alleviant system in patients with HFpEF/HFmrEF.

Provider

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