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Clinical Efficacy in Relief of Dyspnea by HVNI: Evaluation of New Device Equivalence

Dyspnea Clinical Trial

Official title:
Clinical Efficacy in Relief of Dyspnea by HVNI: Evaluation of New Device Equivalence

Clinical Trial Summary

This study will evaluate the ability of a new High Velocity Nasal Insufflation [HVNI] device design to effect ventilation and related physiological responses relative to the current HVNI device design.

Clinical Trial Description

The objective of this study is to evaluate the ability of a new HVNI device to improve ventilation, dyspnea, and related physiological responses relative to the conventional Precision Flow device design, with which there are published clinical outcomes data. It is hypothesized that the new HVNI device design (V2.0) will be comparable at relieving patient dyspnea when compared to the conventional HVNI device design (Precision Flow). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04590014
Study type Interventional
Source Vapotherm, Inc.
Contact
Status Terminated
Phase N/A
Start date January 12, 2022
Completion date July 15, 2022
View Details
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