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Phase 4 Completed N=27 Randomized Treatment

Nu-Mask Intraoral Airway Device Versus Conventional Bag Valve Mask Ventilation Crossover Trial

Source: ClinicalTrials.gov NCT02627001 ↗
Enrolled (actual)
27
Serious AEs
0.0%
Results posted
Jul 2016
Primary outcomePrimary: Received Minute Volume (Liters) as Measured by Wright Respirometer — 6.8; 5.2 Liters — p=<0.001
◆ Published Evidence
No publication linked

No peer-reviewed publication reporting this trial's results has been linked yet. This can indicate results are unpublished — a known publication-bias signal. We re-check periodically.

Summary

This study comprised a randomized cross-over trial of ventilation using the NuMask Intraoral Mask versus conventional Bag Valve Mask in a cadaver model among United States Army combat medics.

Outcome Measures

OutcomeResultp-value
PRIMARY
Received Minute Volume (Liters) as Measured by Wright Respirometer
6.8; 5.2 <0.001 sig

Eligibility Criteria

Inclusion Criteria

  • United States Army Combat Medics

Exclusion Criteria

  • Injuries precluding performance of bag valve mask ventilation
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02627001). 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. Informational only — not medical advice.

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