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Evaluation of Gas Humidification Practices in Patients Under Invasive Mechanical Ventilation (FP950)

L

Laval University

Status

Enrolling

Conditions

Mechanical Fragility
Respiratory Complication
Humidifier Lung

Treatments

Device: MR850
Device: FP950

Study type

Observational

Funder types

Other

Identifiers

NCT06719258
2022-3714

Details and patient eligibility

About

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.

Enrollment

40 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ≥ 18 years old
  • Admitted to intensive care
  • Under invasive mechanical ventilation with the usual indications for the use of a heated humidifier (prolonged invasive mechanical ventilation and / or protective ventilation requiring high respiratory rates.

Exclusion criteria

  • Mechanical venitilation immediately after surgery (<24h)
  • Imminent extubation or planned intubation of very short duration (<24h)
  • Enrolled in the SAVE-ICU study in the group receiving volatile agents with the AnaConDa system.

Trial design

40 participants in 2 patient groups

MR850
Description:
20 subjects on this heating humidifier (Fisher \& Paykel MR850).
Treatment:
Device: MR850
FP950
Description:
20 subjects on this heating humidifier (Fisher \& Paykel FP950).
Treatment:
Device: FP950

Trial contacts and locations

1

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Central trial contact

François Lellouche; Pierre-Alexandre Bouchard

Data sourced from clinicaltrials.gov

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