Comparison of Cardiac Index and Stroke-volume-index Measured by Pulmonary Artery Catheter, FloTrac® and Argos® in Cardiac Surgery Patients.

A comparison of cardiac performance determined by stroke-volume-index measured by different mechanisms in patients during and after cardiac surgery:

1. Pulmonary artery catheter 2. Flo Trac 3. Argos Monitor Investigations will be done in theater and on ICU in ventilated and spontaneously breathing patients.

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Key information

Conditions

Cardiac Failure Acute Hemodynamic Monitoring

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Klinik für Anästhesiologie und Intensivmedizin, Klinikum Karlsburg

Karlsburg, 17495, Germany

Location status: Recruiting

Location contact

Matthias Heringlake

CONTACT

004938355700

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Patient after cardiac surgery with pulmonary artery catheter

Exclusion criteria

Hemodynamic instability, no consent

Treatment and study plan

Measurement of cardiac performance

Diagnostic Test

Measurement of cardiac performance by different devices

Primary outcomes

stroke volume index

Time frame: 24 hours

stroke volume index

Study contacts

Contact information is provided by the study sponsor or research team.

Matthias Heringlake

CONTACT

[email protected]

Deutschland

Sponsors and collaborators

Lead sponsor

Karlsburg Hospital

Other

Registry information

Important dates

Study start: 2025
Primary completion: 2025
Study completion: 2025
First posted: Apr 9, 2025
Registry last updated: Apr 9, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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