Intra-arrest ventilation using the laryngeal tube EVO during continuous resuscitation - a prospective randomized study on human cadavers

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

DRKS

Registry ID

DRKS00037836

Enrollment

Registered

2025-09-09

Start date

2025-10-06

Completion date

Unknown

Last updated

2025-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

R09.2 I46 R09.2

Interventions

Group 1: Four minutes of bag-device ventilation using the laryngeal tube EVO under machine cardiac compression (110/min). Group 2: Four minutes of intermittent-positive-pressure-ventilation using the

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Thiele-fixed corpses of adult body donors: all participants consented during their lifetime to use in the anatomical institute or for scientific studies.

Exclusion criteria

Exclusion criteria: Adult respiratory distress syndrome (ARDS), severe lung or chest injuries, pneumothorax, abnormal airways, tracheostoma, history of severe aspiration

Design outcomes

Primary

Measure	Time frame
The actual applied mean tidal volume (expiratory tidal volume) is measured during the entire 16-minute ventilation period (4x4 minutes) under machine cardiac compression (110/min). The tidal volumes are measured and recorded by the ventilator.	—

Secondary

Measure	Time frame
Difference between ideal and actual applied tidal volume, inspiratory and expiratory tidal volumes, minute ventilation, leakage, respiratory flow curve, pinsp, ppeak, pmean	—

Countries

Germany

Contacts

Public ContactGerrit Jansen

Johannes Wesling Klinikum Minden, Universitätsklinik für Anästhesiologie, Intensiv- und Notfallmedizin

gerrit.jansen@muehlenkreiskliniken.de+49 571 7904401

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026