Simulation of prolonged manual ventilation techniques
Prolonged Manual Ventilation Simulation
This study tests how well different manual breathing devices work during a long simulation to see which one helps people breathe better in emergencies.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 102 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | SafeBVM Industry-sponsored |
| Locations | 1 site (Providence, Rhode Island) |
| Trial ID | NCT06805838 on ClinicalTrials.gov |
What this trial studies
This pilot study evaluates the effectiveness of different manual resuscitation devices in simulated lung scenarios. Participants will use a standard manual resuscitator bag, a flow limiting resuscitator bag, and an FDA-approved flow rate limiting device in a controlled environment. The study aims to assess the performance and outcomes of these devices over a 10-hour simulation period. It is designed for individuals with current basic life support certification to ensure a standardized level of knowledge and skill.
Who should consider this trial
Good fit: Ideal candidates are individuals aged 18 and older with a current basic life support certification.
Not a fit: Patients who have received training in medical or respiratory therapy schools may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance training protocols for manual ventilation, improving patient outcomes in emergency situations.
How similar studies have performed: While this approach is innovative, similar studies have not been widely reported, indicating a novel exploration in this area.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 18 years old or older * Have a current basic life support (BLS) certification * Be available for the entire 10 hours to complete the protocol Exclusion Criteria: * Any training in medical school or respiratory therapy school * Not being available for the full 10 hours to complete the protocol
Where this trial is running
Providence, Rhode Island
- Brown Physicians, Inc — Providence, Rhode Island, United States (Recruiting)
Study contacts
- Principal investigator: Mark Brady, MD — Brown Physicians, Inc.
- Study coordinator: Mark Brady, MD
- Email: mark.brady@brownphysicians.org
- Phone: 4013385284
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.