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

April 5, 2025 updated by: Prof. Dr. Matthias Heringlake, Karlsburg Hospital

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.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Estimated)

40

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

  • Germany
      • Karlsburg, Germany, 17495
        • Recruiting
        • Klinik für Anästhesiologie und Intensivmedizin, Klinikum Karlsburg
        • Contact:
          • Matthias Heringlake
          • Phone Number: 004938355700

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

All patients after cardiac surgery requirering a pulmonary artery catheter

Description

Inclusion Criteria:

  • Patient after cardiac surgery with pulmonary artery catheter

Exclusion Criteria:

  • Hemodynamic instability, no consent

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
stroke volume index
Time Frame: 24 hours
stroke volume index
24 hours

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Karlsburg Hospital

Investigators

  • Principal Investigator: Matthias Heringlake, Head of Department of Anesthesiology and intensive care, Karlsburg Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 1, 2025

Primary Completion (Estimated)

June 1, 2025

Study Completion (Estimated)

December 1, 2025

Study Registration Dates

First Submitted

March 29, 2025

First Submitted That Met QC Criteria

April 5, 2025

First Posted (Actual)

April 9, 2025

Study Record Updates

Last Update Posted (Actual)

April 9, 2025

Last Update Submitted That Met QC Criteria

April 5, 2025

Last Verified

April 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • KAIKB 2025-1

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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