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RECRUITING
NCT05664191
PHASE2

Levosimendan as Treatment of Aneurysmal SubArachnoid Haemorrhage

Sponsor: Assistance Publique - Hôpitaux de Paris

View on ClinicalTrials.gov

Summary

Sub-arachnoid haemorrhage (SAH) are often due to ruptured intracerebral aneurysms and are associated with an importante morbi-mortality. SAH are often complicated by delayed cerebral ischemia (DCI) potentially due to cerebral vasospasm (CVS). A recent study showed that levosimendan, an inotropic and vasodilatory drug, could reduce the incidence of CVS and potentially improve patient outcome. In this pilot randomized controlled trial, we will evaluate the impact Levosimendan vs Placebo in SAH patient on the occurrence of CVS and DCI. Study population: adult patient admitted to ICU for aneurysmal SAH WFNS grade I-IV and mFisher 3-4. Intervention: Levosimendan (0.1 µg/kg/min) or placebo infusion at Day 1 and 8. Primary outcome: incidence of DCI or CVS at day 14 Duration of the study: 24 months Number of patients: 30 (15 patients per group) Number of center: 1

Official title: Use of Levosimendan as Treatment of Aneurysmal SubArachnoid Hemorrhage

Key Details

Gender

All

Age Range

18 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

30

Start Date

2023-10-13

Completion Date

2026-04-13

Last Updated

2025-09-08

Healthy Volunteers

No

Interventions

DRUG

Levosimendan

Infusion at 0.1 µg/kg/min at day 1 and day 8

OTHER

Placebo

Glucose 5%, solution for injection ECOFLAC at day 1 and day 8

Locations (1)

Hôpital Lariboisière, Service d'anesthésie Réanimation

Paris, France, France