Continuous Compressions With Asynchronous Ventilations Using I-gel Device Versus 30:2 Approach During Simulated OHCA

NCT04736446 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2024-11-12

No results posted yet for this study

Summary

Paramedics and EMT will be recruited among four Emergency Medical Services (EMS) in Switzerland to manage a 10-minutes simulation-based adult out-of-hospital cardiac arrest scenario in teams of two. Depending on randomization, each team will manage the scenario according either to their current approach (30 compressions with 2 bag-mask ventilations), or to the experimental approach (continuous compressions since the start of CPR except for rhythm analysis and shock delivering, with early insertion of an i-gel® device to deliver asynchronous ventilations). The main hypothesis is that early insertion of i-gel could improve CCF during out-of-hospital cardiac arrest, with a reasonable time to first effective ventilation.

Conditions

  • Cardiac Arrest
  • Cardiopulmonary Arrest
  • Emergency Medical Services
  • Resuscitation

Interventions

DEVICE

I-gel® supraglottic device

Use of an i-gel® supraglottic device to deliver ventilations

DEVICE

Face mask ventilation

Use of a face mask to deliver ventilations

Sponsors & Collaborators

  • Service de protection et sauvetage Lausanne (SPSL), Emergency Medical Services, Switzerland

    collaborator UNKNOWN
  • Ambulance Riviera, Emergency Medical Services, La Tour-de-Peilz, Switzerland

    collaborator UNKNOWN
  • Compagnie d'Ambulances de l'Hôpital du Valais, Emergency Medical Services, Martigny, Switzerland

    collaborator UNKNOWN
  • Swissrescue.ch, Website for Prehospital Healthcare Providers, Les Pontins, Switzerland

    collaborator UNKNOWN
  • ESAMB - College of Higher Education in Ambulance Care, Geneva, Switzerland

    collaborator UNKNOWN
  • STAR Ambulances, Emergency Medical Services, Épalinges, Vaud

    collaborator UNKNOWN
  • Geneve TEAM Ambulances

    lead OTHER

Principal Investigators

  • Loric Stuby · Genève TEAM Ambulances

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-02-14
Primary Completion
2021-05-18
Completion
2021-05-18

Countries

  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04736446 on ClinicalTrials.gov