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Pilot Study Comparing Ventilation Modes During CPR With Mechanical Compression Device. — COVME  

Cardiopulmonary Resuscitation Clinical Trial

Official title:
Pilot Study: Comparison of Ventilation Modes During Cardio-pulmonary Resuscitation With a Mechanical Compression Device in the Emergency Room

Clinical Trial Summary

Comparison of three ventilation modes (volume controlled, BIPAP and CPAP) during cardiopulmonary re-suscitation with a mechanical compression device in the emergency room. Primary aim is to assess mean ventilation volume in the first 15 minutes after randomization.

Clinical Trial Description

Mechanical compression devices are applied to grant continuous chest compressions and consequently blood flow during CPR (cardiopulmonary rescuscitation). Current guidelines, however, are lacking guidance of the optimal ventilation strategy in such scenarios. This may lead to lung injuries caused by high pressure levels in the chest while applying compression and ventilation simultaneously or hypoventilation. Consequently, this pilot study assesses iwhich ventilation mode is optimal. Patients will be assigned randomly to one of the three ventilation modes (Volume controlled, BiPAP-ASB, CPAP). Ventilation parameters will be continuously monitored for 15 minutes while blood gas analyses are taken as well. Further secondary outcome parameters will be assessed, e.g. hospital mortality. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03347175
Study type Interventional
Source Technische Universität München
Contact
Status Completed
Phase N/A
Start date November 6, 2017
Completion date December 12, 2019
View Details
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