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Nasal Airflow to Modulate Dyspnea in Tracheostomized Patients

Study acronym: MODUS
StatusRecruiting
PhaseNot applicable
Started2026-02-17
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 11 months later Feb 2027 → Feb 2028
See other at-risk trials from Assistance Publique - Hôpitaux de Paris

Amendment history

2026-09-30
Recruitment opened
Primary completion pushed: 2027-02 → 2028-02
Completion pushed: 2027-02 → 2028-02
2026-01-27
Study Status v2
Re-verified, no change to tracked fields
2025-12-29
Study Status, Study Design, Arms and Interventions, Outcome Measures v1
InterventionsBaseline (Procedure), FAN (Procedure), Installation of high flow humidified air cannula (Procedure), Nasal air puffs (Procedure)→Baseline (Procedure), Installation of high flow humidified air cannula (Procedure), Nasal air puffs (Procedure), propeller fan (FAN)…
Secondary endpoints4 entries, revised
respiratory electromyogram (EMG)
2025-12-15
Original filing
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.
Trial Details
NCT Number NCT07308171
Lead Sponsor Assistance Publique - Hôpitaux de Paris
Conditions Ventilated Patients
Enrollment 24 participants
Start Date 2026-02-17
Primary Completion 2028-02 (estimated)
Study Completion 2028-02 (estimated)
Updated on ClinicalTrials.gov 2026-09-29