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REDUCE LAP-HF III Corvia Protocol 1701 — REDUCELAPHFIII  

Heart Failure Clinical Trial

Official title:
A Post-Market Clinical Follow-up Study to Evaluate the Corvia Medical, Inc. InterAtrial Shunt Device - IASD® System II to REDUCE Elevated Left Atrial Pressure in Patients With Heart Failure

Clinical Trial Summary

This is a post market trial to be conducted at sites in Germany. The device has CE approval in the EU. The purpose of this observational registry is to collect post market data in consecutive patients treated with the IASD System II, to further evaluate efficacy, safety and quality of life outcomes as a new treatment for patients with heart failure in a "real world" practice setting.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03191656
Study type Observational
Source Corvia Medical
Contact Jan Komtebedde, DVM
Phone 978-654-6113
Email jkomtebedde@corviamedical.com
Status Recruiting
Phase
Start date July 12, 2017
Completion date July 31, 2028
View Details
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