Stroke volume variation derived from uncalibrated pressure waveform analysis for the prediction of fluid responsiveness in cardiac surgical patients with impaired left ventricular functio

Withdrawn

• Conditions: Prediction of fluid responsiveness; 10019280

• Registration Number: NL-OMON32328
• Lead Sponsor: niversitair Medisch Centrum Utrecht

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 6 May 2024

Recruitment & Eligibility

• Status: Withdrawn
• Sex: Not specified
• Target Recruitment: 34

Inclusion Criteria

34 elective cardiac surgical patients with a left ventricular ejection fraction < 35% will be included in each center.

Exclusion Criteria

Excluded will be patients with major vascular diseases (aortic aneurysm and or peripheral arterial vascular surgery), intracardiac shunts, esophageal dysfunction, and patients undergoing emergency surgery.

Study & Design

• Study Type: Observational invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Monitoring of cardiac output, bloodpressure, heart rate and stroke volume<br /><br>variation before and after the administration of 7 ml/kg hydroxyethyl starch 6%<br /><br>in patients in the operating theatre and the intensive care. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>not applicable</p><br>