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

NACompletedINTERVENTIONAL
Enrollment

26

Participants

Timeline

Start Date

October 1, 2020

Primary Completion Date

June 7, 2022

Study Completion Date

June 7, 2022

Conditions
DyspneaHypercapniaRespiratory Insufficiency
Interventions
DEVICE

Control Cannula - Prosoft Cannula - Unicorn Cannula

The purpose of this intervention is to evaluate the efficacy of a conventional legacy cannula design to provide targeted relief of dyspnea. The purpose of this intervention is to evaluate the efficacy of a next generation cannula to provide relief of dyspnea.

DEVICE

Control Cannula - Unicorn Cannula - Prosoft Cannula

The purpose of this intervention is to evaluate the efficacy of a conventional legacy cannula design to provide targeted relief of dyspnea. The purpose of this intervention is to evaluate the efficacy of a next generation cannula to provide relief of dyspnea.

Trial Locations (2)

15240

VA Pittsburgh Healthcare System, Pittsburgh

37403

Erlanger Baroness Hospital, Chattanooga

All Listed Sponsors
collaborator

VA Pittsburgh Healthcare System

FED

collaborator

Erlanger Baroness Hospital

OTHER_GOV

lead

Vapotherm, Inc.

INDUSTRY

NCT04512781 - Clinical Efficacy in Relief of Dyspnea by HVNI: Evaluation of New Cannulae Designs | Biotech Hunter | Biotech Hunter