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Intra-Arrest-Ventilation in Human Cadavers

NCT06306898 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2025-03-17

No results posted yet for this study

Summary

The study investigates the influence of non-synchronized bag-device-ventilation and intermittent positive pressure ventilation (IPPV), as recommended in the current resuscitation guidelines of the European Resuscitation Concil (tidal Volume (Vt) = 5-6 mL/kg body weight, respiratory rate = 10 min-1) and Chest Compression Synchronized Ventilation (pInsp = 40 mbar; respiratory rate = chest compression rate) with regard to achieving a sufficient tidal volume and the tightness of various supraglottic airway devices (laryngeal mask, i-Gel-laryngeal mask, laryngeal tube) and endotracheal intubation.

Conditions

  • Cardiac Arrest

Interventions

OTHER

Endotracheal Intubation

Ventilation with an endotracheal tube

OTHER

Laryngeal tube

Ventilation with an laryngeal tube

OTHER

Laryngeal mask

Ventilation with an laryngeal mask

OTHER

I-Gel-Laryngeal Mask

Ventilation with an I-Gel-laryngeal mask

Sponsors & Collaborators

  • Ruhr University of Bochum

    collaborator OTHER

  • Bielefeld University

    collaborator OTHER

  • Gerrit Jansen

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-03-18
Primary Completion
2024-08-21
Completion
2024-08-21

Countries

  • Germany

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 NCT06306898 on ClinicalTrials.gov