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Effect of Adding Vasopressin on Cardiac Output, Blood Pressure, Diuresis, and Tissue Perfusion Indices in Patients With Septic Shock
Sponsor: Assistance Publique - Hôpitaux de Paris
Summary
In patients with septic shock, vasopressin is increasingly used in combination with norepinephrine, but its timing of initiation remains heterogeneous and its clinical hemodynamic effects are still insufficiently characterized. Available data suggest variable responses, which may depend on the hemodynamic phenotype at the time of treatment initiation. In particular, the effects of vasopressin may differ according to the presence of preload dependency, baseline cardiac output, impaired systolic function, or baseline diastolic arterial pressure, reflecting the degree of vasoplegia. In this context, the VASO-PHENO study aims to provide a detailed and dynamic description of the early hemodynamic and clinical effects of vasopressin initiation in septic shock. To date, no clinical study has systematically and dynamically evaluated the effects of vasopressin on central and peripheral hemodynamic parameters according to the hemodynamic profile at the time of its initiation. Describing these effects appears essential to better understand the variability in clinical responses and to contribute to a more rational and personalized approach to vasopressor escalation in septic shock.
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
200
Start Date
2026-08-01
Completion Date
2029-09-01
Last Updated
2026-07-13
Healthy Volunteers
No
Conditions
Locations (8)
CHU d'Angers
Angers, France
CH de Dieppe
Dieppe, France
Hôpital Bicêtre
Le Kremlin-Bicêtre, France
GHE, Hôpital Louis Pradel, HCL
Lyon, France
GHS - Hôpital Lyon Sud, HCL
Lyon, France
Hôpital Nord, AP-HM
Marseille, France
CHU Rennes - Site Pontchaillou
Rennes, France
Hôpital Hautepierre, Hôpitaux Universitaires de Strasbourg
Strasbourg, France