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Study identifier: NCT07724262 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Evaluation of the Argos System to Estimate Cardiac Output

Condition: Shock  ·  Sponsor: Bicetre Hospital

PhaseN/A
Planned participants120
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Christopher Lai, MD, PhD  ·  12633816521  ·  christopher.lai@aphp.fr

Always discuss trial participation with your own doctor first.

Locations (1)

Bicêtre HospitalLe Kremlin-Bicêtre, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT07724262