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Evaluation of the Safety and Efficacy of TLD in Patients With COPD — AIRFLOW-3  

COPD Clinical Trial

Official title:
A Multicenter, Randomized, Sham-controlled Study to Evaluate Safety and Efficacy After Treatment With the Nuvaira™ Lung Denervation System in Patients With Chronic Obstructive Pulmonary Disease (COPD)

Clinical Trial Summary

The purpose of this study is to confirm the safety and efficacy of the Nuvaira Lung Denervation System (Nuvaira System) in the treatment of COPD.

Clinical Trial Description

The primary objective of this study is to demonstrate the superiority of treatment with the Nuvaira Lung Denervation System (Active Treatment arm) compared to a sham procedure (Sham Control arm) to decrease moderate or severe exacerbations in subjects with COPD on optimal medical care. The secondary objective is to compare long-term safety, and other efficacy assessments between the Active Treatment arm and the Sham Control arm. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03639051
Study type Interventional
Source Nuvaira, Inc.
Contact
Status Active, not recruiting
Phase N/A
Start date May 23, 2019
Completion date September 2028
View Details
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