LANdiolol MIcrocirculatory Effects During Septic chOc (MILANOS)
Condition(s) studied
Investigational drug(s) / intervention(s)
Landiolol: Intravenous Landiolol injection (from 0.5 to 10 µg/kg/min during 12 hours) up to a 15% decrease in HR on microcirculatory vascular reactivity.
Study summary
The objectives of this study are to evaluate the effect of continuous intravenous Landiolol injection (from 0.5 to 10 µg/kg/min during 12 hours ) up to a 15% decrease in Heart Rate (HR) on microcirculatory vascular reactivity vs. usual tachycardia management and evaluate the hemodynamic effects of Landiolol vs. usual management in patients with septic shock.
Eligibility
Primary outcome measure(s)
- Rate of decrease in heart rate (HR) on microcirculatory vascular reactivity — 24 hours
The objectives of this study are to evaluate the effect of continuous intravenous Landiolol injection (from 0.5 to 10 µg/kg/min during 12 hours ) up to a 15% decrease in HR on microcirculatory vascular reactivity vs. usual tachycardia management in patients with septic shock.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Intensive care department, Hôpital Saint Antoine | Paris | France | Recruiting |
More Assistance Publique - Hôpitaux de Paris trials in France
Other trials for the same condition
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 NCT04931225 on ClinicalTrials.gov ↗ ← All trials in France