Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT07066566

The Effect of Asymmetrical vs. Symmetrical High Flow Nasal Cannula on the Work of Breathing

Led by Larissa University Hospital · Updated on 2025-07-18

30

Participants Needed

1

Research Sites

72 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this study randomized single-center crossover study is to evaluate the impact of asymmetrical versus symmetrical nasal high flow (NHF) therapy on work of breathing (WOB). The main question it aims to answer are: 1\. Does the asymmetrical NHF interface improve the work of breathing compared to the symmetrical NHF interface? Researchers will compare the symmetrical NHF interface to the symmetrical NHF interface to see if the the asymmetrical interface has a greater impact on the work of breathing. Participants will : 1. receive NHF via both interfaces (FiO₂ 0.21, 50 L/min) for 15 minutes, in random order, with esophageal pressure monitoring and bioelectrical impedance analysis performed. 2. baseline characteristics will me monitored throughout the interventions 3. Esophageal pressure and minute ventilation will be monitored.

CONDITIONS

Official Title

The Effect of Asymmetrical vs. Symmetrical High Flow Nasal Cannula on the Work of Breathing

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • No symptoms or signs of respiratory failure (oxygen saturation above 95% on room air)
Not Eligible

You will not qualify if you...

  • Pregnancy
  • Oxygen saturation below 94% on room air
  • Neuromuscular disease
  • Contraindications to esophageal pressure monitoring such as uncontrolled bleeding, esophageal disease, nasal injury, or allergy to local lidocaine

AI-Screening

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Trial Site Locations

Total: 1 location

1

University Hospital of Larissa, Department of Pulmonary Medicine

Larissa, Greece, 41222

Actively Recruiting

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Research Team

I

Ioannis Dr. Pantazopoulos, Associate Professor

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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