ongitudinal comparison of cardiac stroke volume measured by pulse contour analysis and echocardiography in patients with acute respiratory distress syndrome managed with and without extracorporal membrane oxygenatio

Not Applicable

Recruiting

• Conditions: J80; Adult respiratory distress syndrome

• Registration Number: DRKS00028584
• Lead Sponsor: Geschäftsfeldleiter Intensivmedizin Klinik für Anästhesiologie und Operative IntensivmedizinUniversitätsmedizin Mannheim

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2022-03-28
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

severe acute respiratory failure managed with ECMO
- Control group: patients with severe acute respiratory failure managed without ECMO
- Informed consent of patient/ next of kin
- central venous and arterial catheter in place

Exclusion Criteria

- age under 18 years
- congenital malformation, severe valve dysfunction, severe arrhythmia
- predicted survival less than 24 hours

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Comparing measurement of cardiac stroke volume at six hours with transthoracic echocardiography and pulse contour analysis in patients with severe ARDS managed with and without ECMO

Secondary Outcome Measures

Name	Time	Method
Comparing measurement of cardiac stroke volume at three hours with transthoracic echocardiography and pulse contour analysis in patients with severe ARDS managed with and without ECMO<br>