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Evaluation of the Argos System to Estimate Cardiac Output

Recruitingn/aAges 18 Years - anyAllBicetre Hospital
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In plain words

What the trial is, and whether it could suit you

The goal of this observational study is to evaluate the reliability of the Argos system to track changes in cardiac output in critically ill patients. The main question it aims to answer is: Does cardiac output changes induced by fluid administration or changes in norepinephrine dosage can be tracked by the Argos system, compared to transpulmonary thermodilution device.

Sign in to get the eligibility rules as simple questions to take to your doctor.

📋 Eligibility rules (as published)
Inclusion Criteria: * Age ≥18 years old * Hospitalisation in intensive care * Haemodynamic monitoring with transpulmonary thermodilution already in place * Hemodynamic intervention deemed necessary by the clinician in charge of the patient * Administration of a fluid bolus * Change in norepinephrine dosage or performance of a vasopressor test Exclusion Criteria: * Pregnancy * Other therapeutic modification during volume expansion or the vasopressor test * Refusal to participate by relatives of the patient or the patient himself or herself * Non availability of investigators
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What it tests

  • Fluid bolus
  • Norepinephrine
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Where

1 site
Bicêtre Hospital
Le Kremlin-Bicêtre, France
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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