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RECRUITING
NCT06836908

CCSV - Post Market Clinical Follow-up Study

Sponsor: Medical University of Vienna

View on ClinicalTrials.gov

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.

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

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

98

Start Date

2024-06-01

Completion Date

2026-09

Last Updated

2025-02-20

Healthy Volunteers

No

Conditions

Locations (1)

Medical University of Vienna

Vienna, Austria, Austria