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

NCT ID: NCT05709613

Last Updated: 2023-09-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

34 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-01-30

Study Completion Date

2023-06-13

Brief Summary

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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.

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Detailed Description

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Conditions

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Cardiac Arrest Cardiopulmonary Arrest Resuscitation Emergency Medicine

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors
Data extraction will be fully automated and the statistician will not know the identity of the participants or the sequence they were allocated to.

Study Groups

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No feedback device

This group will have no access to the feedback device

Group Type NO_INTERVENTION

No interventions assigned to this group

Feedback device

This group will have access to the feedback device

Group Type EXPERIMENTAL

Use of a chest compressions' feedback device

Intervention Type DEVICE

The participants will have access to a chest compressions' feedback device

Interventions

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Use of a chest compressions' feedback device

The participants will have access to a chest compressions' feedback device

Intervention Type DEVICE

Eligibility Criteria

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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.
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Geneve TEAM Ambulances

OTHER

Sponsor Role lead

Responsible Party

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Stuby Loric

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Loric Stuby

Role: PRINCIPAL_INVESTIGATOR

Genève TEAM Ambulances

Locations

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ACE Genève Ambulances

Chêne-Bougeries, Canton of Geneva, Switzerland

Site Status

Ambulances de la Ville de Sion

Sion, Valais, Switzerland

Site Status

Genève TEAM Ambulances

Geneva, , Switzerland

Site Status

SK Ambulances

Geneva, , Switzerland

Site Status

Countries

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Switzerland

Related Links

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https://swiss-cpr-studies.ch/

Whole project website

Other Identifiers

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CPR-7

Identifier Type: -

Identifier Source: org_study_id

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