Effect of Adding Vasopressin on Cardiac Output, Blood Pressure, Diuresis, and Tissue Perfusion Indices in Patients With Septic Shock
Condition(s) studied
Study 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.
Eligibility
Primary outcome measure(s)
- To describe and compare the evolution of cardiac index between inclusion and 20 minutes after vasopressin initiation in patients with septic shock, according to hemodynamic profiles identified a posteriori from variables collected at the time of vasopre — T0 = inclusion. T20 = 20 minutes after the introduction of the vasopressin
Hemodynamic profiles will not be defined a priori. They will be identified a posteriori using a supervised clustering analysis based on variables measured at inclusion and selected for their pathophysiological relevance: * presence of preload dependency at the time of vasopressin initiation (yes/no); * cardiac index at inclusion; * diastolic arterial pressure at inclusion; * left ventricular ejection fraction (LVEF).
Trial sites (8)
| Facility | City | Region | Status |
|---|---|---|---|
| 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 |
More Assistance Publique - Hôpitaux de Paris trials in France
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07697144 on ClinicalTrials.gov ↗ ← All trials in France