Trials / Recruiting
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.