Actively Recruiting

Age: 18Years +
All Genders
ID06918301

Comparison of Cardiac Index and Stroke-volume-index Measured by Pulmonary Artery Catheter, FloTracae and Argosae in Cardiac Surgery Patients

Led by Karlsburg Hospital · Updated on 2025-04-09

40

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating cardiac performance by comparing stroke-volume-index measurements taken by three different methods in patients undergoing and recovering from cardiac surgery. The study focuses on patients after cardiac surgery who have a pulmonary artery catheter and involves monitoring during surgery and in the intensive care unit, including both ventilated and spontaneously breathing patients. The study assesses cardiac performance using three diagnostic tools: the pulmonary artery catheter, FloTrac, and the Argos Monitor. These devices measure cardiac output and stroke-volume-index by different mechanisms. Investigations are conducted in the operating theater and intensive care unit to observe measurements under various patient conditions. Participants will be monitored for stroke volume index over a 24-hour period following surgery. The study collects data using these devices without altering patient treatment. Researchers will evaluate and compare the measurements to understand differences among the methods. This observational study does not include treatments or interventions beyond standard care, and participation duration depends on the postoperative monitoring period.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient after cardiac surgery with pulmonary artery catheter
Not Eligible

You will not qualify if you...

  • Hemodynamic instability
  • No consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - 24 hours

Participants undergo measurement of cardiac performance using different devices after cardiac surgery.

1 hospital stay with continuous monitoring

Long-term Monitoring

Duration - Up to 24 hours after surgery

Participants are observed following diagnostic measurements to assess cardiac function.

Monitoring during hospital stay

Trial Site Locations

Total: 1 location

1

Klinik für Anästhesiologie und Intensivmedizin, Klinikum Karlsburg

Karlsburg, Germany, 17495

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Research Team

M

Matthias Heringlake

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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