N/A
N=32
Manual Ventilation Efficacy With MVG Device
Ventilator Lung
Bottom Line
View on ClinicalTrials.gov: NCT05059366 ↗Enrolled (actual)
32
Serious AEs
0.0%
Results posted
Jul 2022
Primary outcome: Primary: Tidal Volume — 502.030; 492.508; 478.889; 481.533 mL
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Manual Ventilation Grip Device (Device); 2VE (Other)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- University of Miami
- Primary completion
- Aug 2021
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Tidal Volume |
502.030; 492.508; 478.889; 481.533 | — |
| SECONDARY Fatigue as Measured by NASA-TLX Questionnaire |
33.92; 53.69; 42.54; 63.69 | — |
| SECONDARY Fatigue as Measured by SOFI Questionnaire |
13.08; 17.13; 16.38; 23.28 | — |
Summary
The purpose of this research is to investigate the efficacy of the newly designed ventilation grip device (MVG device).
Eligibility Criteria
Inclusion Criteria
- Current medical students, Post Graduate Year 1 (PGY1) residents or residents from other specialties with no prior experience in hand mask ventilation techniques or anesthesiology residents and attendings with at least 2 or more years of clinical experience
Exclusion Criteria
- Refusal to participate in the study.
- Medical students with prior experience in hand mask ventilation techniques (i.e. experiences in previous careers such as nursing or Emergency Medical Technician (EMT) professions)
- Any physical inability to adequately perform ventilation
Data sourced from ClinicalTrials.gov (NCT05059366). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.