Ireland
--:--IST
Starting soon Observational

Effect of Adding Vasopressin on Cardiac Output, Blood Pressure, Diuresis, and Tissue Perfusion Indices in Patients With Septic Shock

NCT07697144 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2026-08-01
Last updated
2026-07-13

Condition(s) studied

Septic Shock and Use of Vasopressin

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

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age ≥ 18 years; * Hospitalized in an intensive care unit; * Presenting with septic shock according to Sepsis-3 criteria; * For whom the treating clinician wishes to initiate vasopressin as second-line therapy as part of routine care; * Undergoing hemodynamic monitoring with a PiCCO2 device (Pulsion Medical Systems, Getinge, Feldkirchen, Germany) or pulmonary artery catheterization as part of routine care. Exclusion Criteria: * Patient already receiving vasopressin; * Pregnancy; * Patient under legal protection; * Patient unwilling to participate in the study.

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)

FacilityCityRegionStatus
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
Official registry record

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