Comparing methods to measure heart performance in cardiac surgery patients
Official title: Comparison of Cardiac Index and Stroke-volume-index Measured by Pulmonary Artery Catheter, FloTrac® and Argos® in Cardiac Surgery Patients.
Run by Karlsburg Hospital · NCT06918301 · Data updated 2026-11-12
This study is testing three different ways to measure heart performance in patients having heart surgery to see which method works best.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 40 (estimated) |
| Sponsor | Karlsburg Hospital Academic / other |
| Locations | 1 site (Karlsburg) |
| Status | Recruiting |
| Started | March 1, 2025 |
| Main results expected | June 1, 2025 |
| Study ends | December 1, 2025 |
| Registry record updated | April 9, 2025 |
| Trial ID | NCT06918301 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are patients who have undergone cardiac surgery and have a pulmonary artery catheter in place.
✕Probably not a fit
Patients experiencing hemodynamic instability or those who cannot provide consent may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to compare cardiac performance in patients undergoing cardiac surgery by measuring stroke-volume-index using three different methods: pulmonary artery catheter, FloTrac®, and Argos®. Investigations will take place in the operating theater and ICU, involving both ventilated and spontaneously breathing patients. The study will help determine the most effective method for hemodynamic monitoring in this patient population.
Why it matters
Potential benefit: If successful, this study could improve the accuracy of cardiac performance monitoring in patients undergoing cardiac surgery.
How similar studies have gone: While there have been studies on hemodynamic monitoring, this specific comparison of these three methods in cardiac surgery patients is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patient after cardiac surgery with pulmonary artery catheter Exclusion Criteria: * Hemodynamic instability, no consent
Where it's running
-
Klinik für Anästhesiologie und Intensivmedizin, Klinikum Karlsburg
Karlsburg, Germany Recruiting
Study contacts
- Principal investigator: Matthias Heringlake — Head of Department of Anesthesiology and intensive care, Karlsburg Hospital
- Study coordinator: Matthias Heringlake
- Email: heringlake@t-online.de
- Phone: Deutschland
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.