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ALLEVIATE-HF-HD Study

Heart Failure Clinical Trial

Official title:
Evaluation of the Safety and Efficacy of a Percutaneously Created Interatrial Shunt in Patients With Chronic Heart Failure Without Pulmonary Vascular Disease

Clinical Trial Summary

Patients with heart failure and reduced left ventricular ejection fraction (HFrEF, EF 25-39%), or mid-range left ventricular ejection fraction (HFmrEF, EF 40-49%), or preserved left ventricular ejection fraction (HFpEF, EF ≥ 50%), with mild to moderate functional limitation will be evaluated for treatment via creation of a no-implant interatrial shunt using clinical, echocardiographic, and invasive hemodynamic data.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05501652
Study type Interventional
Source Alleviant Medical, Inc.
Contact
Status Completed
Phase Phase 1
Start date June 30, 2022
Completion date February 3, 2023
View Details
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