Nasal Airflow to Modulate Dyspnea in Tracheostomized Patients

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorAssistance Publique - Hôpitaux de Paris

About this trial

The hypothesis of the present study is that restoring nasal stimulation alleviates dyspnea and improves respiratory drive. The aim of this study is to compare three non-pharmacological approaches designed to restore nasal stimulation (continuous nasal airflow, nasal sprays, and facial airflow) in tracheotomized patients dependent on mechanical ventilation.

Eligibility criteria

Qualifiers

Age ≥ 18 years

Tracheostomy and mechanical ventilation

Dyspnea ≥3

Consent to participate

Disqualifiers

Agitation, delirium

Continuous use of sedatives

Patients under law protection

Inmates

Trial design

Treatments tested in this trial

  • Baseline
  • Installation of high flow humidified air cannula
  • Nasal air puffs
  • propeller fan (FAN)

Treatment groups

24 Participants
are divided into 1 treatment group

Locations

This trial has no locations