Prediction and monitoring of cardiac response to intravenous fluid administration by non-invasive measurement of the initial systolic time interval after cardiac surgery

Recruiting

• Conditions: coronary artery disease; heart monitoring; 10011082

• Registration Number: NL-OMON33850
• Lead Sponsor: Vrije Universiteit Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 6 May 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: 35

Inclusion Criteria

Intensive-care patients who are presumably hypovolaemic and who have a clinical reason for fluid administration.

Exclusion Criteria

Younger than 18 or older than 80 years of age; medical, practical or ethical drawbacks or objections to participate. Blood loss by bleeding at a rate of over 100 ml/h. Relevant alterations in inotropic and vasopressor medication.

Study & Design

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

Primary Outcome Measures

Name	Time	Method
<p>The study parameters are: PEP and the respiratory change delta-PEP, ISTI and<br /><br>delta-ISTI and cardiac output CO. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>None</p><br>