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Use of a Feedback Device to Limit Too Shallow Compressions Associated With the Use of an I-gel® Device

G

Geneve TEAM Ambulances

Status

Completed

Conditions

Emergency Medicine
Cardiopulmonary Arrest
Cardiac Arrest
Resuscitation

Treatments

Device: Use of a chest compressions' feedback device

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Airway management in out-of-hospital cardiac arrest is still debated. Several options exist: bag-valve-mask ventilation, supraglottic devices and endotracheal intubation. Intermediate and advanced airway management strategies could be useful devices to increase chest compression fraction. A previous study shows that early insertion of an i-gel device significantly increases chest compression fraction and enhances respiratory parameters. However, the compressions were found to be shallower in the experimental group using the i-gel device. Although, the shallower compressions found in the supraglottic airway device group did not appear to be linked to their provision in an over-the-head position, it is reasonable to assume that the addition of a feedback device to the use of an i-gel® device could fix this issue. The feedback devices seem to be able to provide a benefit, and allow deeper compressions / more often in the depth target. There is a mismatch between perceived and actual cardiopulmonary resuscitation performance supporting the need for such a feedback device's study.

Enrollment

34 patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Registered EMTs and paramedics actively working in any of the participating study trial centers will be eligible for inclusion.

Exclusion criteria

  • Members of the study team
  • EMTs will be randomly excluded if there are more EMTs than paramedics.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

34 participants in 2 patient groups

No feedback device
No Intervention group
Description:
This group will have no access to the feedback device
Feedback device
Experimental group
Description:
This group will have access to the feedback device
Treatment:
Device: Use of a chest compressions' feedback device

Trial contacts and locations

4

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Data sourced from clinicaltrials.gov

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