ClinicalTrials.govNCT06805838Enrolling by Invitation
Registry Record
View on ClinicalTrials.gov · NCT06805838 →
Study at a Glance
- Registered title: Prolonged Manual Ventilation Simulation
- Sponsor: SafeBVM, with the U.S. Department of Defense as collaborator
- Setting: Simulated lung scenarios, Brown Physicians, Inc., Providence, RI
- Design (per registry): Randomized comparison of a standard manual resuscitator bag, a flow-limiting resuscitator bag, and Sotair® paired with a standard manual resuscitator
- Primary outcome: Minute ventilation while manually ventilating the simulated lung
- Registry status: Enrolling by invitation
Results
Not yet published. When results are published, a summary will be added to the Papers section.
Details are shown as listed on ClinicalTrials.gov (last update posted 2025-08-28). See the registry record for the current status.
Sotair® is FDA 510(k) cleared (K212905) for use in non-breathing adults and is intended to minimize gastric inflation during manual ventilation. Refer to the Instructions for Use for indications, contraindications, warnings and precautions. SotairIQ™ is for training and education use only. This page lists a registered study for healthcare professionals. The registry record is the authoritative source for study details.