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Clinical Efficacy in Relief of Dyspnea by HVNI: Evaluation of New Cannulae Designs

Dyspnea Clinical Trial

Official title:
Clinical Efficacy in Relief of Dyspnea by HVNI: Evaluation of New Cannulae Designs

Clinical Trial Summary

This study will evaluate the ability of High Velocity Nasal Insufflation [HVNI] next generation nasal cannula designs to effect ventilation and related physiological responses relative to the conventional legacy cannula design.

Clinical Trial Description

The objective of this study is to evaluate the ability of HVNI next generation nasal cannula designs to effect ventilation and related physiological responses relative to the current cannula design, with which there are published clinical outcomes data. It is hypothesized that next generation nasal cannula designs (Prosoft and Unicorn) will be comparable at relieving patient dyspnea while on HVNI, when compared to the conventional (Legacy) cannula. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04512781
Study type Interventional
Source Vapotherm, Inc.
Contact
Status Completed
Phase N/A
Start date October 1, 2020
Completion date June 7, 2022
View Details
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