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.