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RecruitingNCT06836908

CCSV - Post Market Clinical Follow-up Study

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

Status
Recruiting
Phase
Study type
Observational
Enrollment
98 (estimated)
Sponsor
Medical University of Vienna · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Conditions

Timeline

Start date
2024-06-01
Primary completion
2026-06-01
Completion
2026-09-01
First posted
2025-02-20
Last updated
2025-02-20

Locations

1 site across 1 country: Austria

Source: ClinicalTrials.gov record NCT06836908. Inclusion in this directory is not an endorsement.