RecruitingNCT06719258

Evaluation of Gas Humidification Practices in Patients Under Invasive Mechanical Ventilation

Evaluation of Gas Humidification Practices in Patients Under Invasive Mechanical Ventilation: Benefit of the F & P950 Heated Humidifier: Comparison With the MR 850 on Clinical Events of Under-humidification


Sponsor

Laval University

Enrollment

40 participants

Start Date

Sep 20, 2024

Study Type

OBSERVATIONAL

Conditions

Summary

When mechanical ventilation is initiated, a humidification method should be chosen. There is two methods: heat and humidity exchanger filters or heated humidity. The second method is recognized to be more efficient, but many external factors can influence its performance. Insufficient humidity results in observable problems, such as difficult management of respiratory secretions. The study compare two heated humidifiers already used in ICU. Data will be collected retrospectively from June 1, 2021.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a medical device called FP950 and a medical device called MR850 for people with humidifier lung, mechanical fragility, and other related conditions. The study is currently recruiting participants at 1 location.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DEVICEMR850

This humidifier will be used straight away for patients whose intubation is expected to last longer than 24 hours.

DEVICEFP950

This humidifier will be used straight away for patients whose intubation is expected to last longer than 24 hours.


Locations(1)

Institut Universitaire de Cardiologie et de Pneumologie de Québec

Québec, Quebec, Canada

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06719258


Related Trials