Cardiac Arrest Clinical Trials

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Chest Compression Synchronized Ventilation (CCSV) - an Exploratory Post Market Clinical Follow-up Study

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

The main goal of this observational study is the evaluation of Chest Compression Synchronized Ventilation (CCSV) regarding oxygenation in terms of PaO2 assessed by routine blood gas analysis, hemodynamic effects, 30-day outcome and safety in comparison to Intermittent Positive Pressure Ventilation (IPPV) as data in humans is sparse especially in direct comparison to other ventilation modes. Cardiac arrest patients in Vienna, Austria will be preclinically randomized (IPPV and CCSV) and ventilated accordingly during CPR. Differences in oxygenation, decarboxylation, systemic perfusion and cerebral oxygenation, the patient's 30-day outcome as well as ventilator-associated adverse events (e.g., pneumothorax) will be recorded and analyzed.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• OHCA

• Correct endotracheal intubation (seen by capnography)

• The patient is being treated by the Vienna Emergency Medical Services within the scope of emergency ventilation.

• MEDUMAT Standard from Weinmann Emergency is used.

• Mechanical ventilation is performed according to the specified indications.

Locations
Other Locations
Austria
Medical University of Vienna
RECRUITING
Vienna
Contact Information
Primary
Sebastian Schnaubelt, MD, PhD
sebastian.schnaubelt@meduniwien.ac.at
+43 1 40400
Time Frame
Start Date: 2024-06-01
Estimated Completion Date: 2026-09
Participants
Target number of participants: 98
Treatments
IPPV
Cardiac arrest patients ventilated with IPPV
CCSV
Cardiac arrest patients ventilated with CCSV
Related Therapeutic Areas
Sponsors
Collaborators: WEINMANN Emergency, Medical Technology GmbH & Co. KG, Berufsrettung Wien
Leads: Medical University of Vienna

This content was sourced from clinicaltrials.gov