Recruiting NCT06918301
Comparison of Cardiac Index and Stroke-volume-index Measured by Pulmonary Artery Catheter, FloTrac® and Argos® in Cardiac Surgery Patients.
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Measurement of cardiac performance.
- Who it may be relevant to
- Registry conditions: Cardiac Failure Acute, Hemodynamic Monitoring. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Germany
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
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.
Interventions
- Diagnostic test Measurement of cardiac performance
Measurement of cardiac performance by different devices
Primary outcome measures
- stroke volume index [Time frame: 24 hours]
Eligibility criteria
Inclusion criteria
- Patient after cardiac surgery with pulmonary artery catheter
Exclusion criteria
- Hemodynamic instability, no consent
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Case-control
Study locations
Germany · 1 center
- Klinik für Anästhesiologie und Intensivmedizin, Klinikum Karlsburg — Karlsburg
Identifiers
NCT: NCT06918301 · KAIKB 2025-1