Clinical Trial

Palmitoylethanolamide and Luteolin in Patients with Acute Ischemic Stroke

Not Yet Recruiting
View on ClinicalTrials.gov →
Summary
Acute ischemic stroke is caused by reduced blood supply to the brain associated with neuroinflammation. This mechanism contributes to acute neuronal death and persists even after reopening of the closed vessel, with consequent limitation of clinical and functional improvement. Experimental and clinical evidence demonstrated the anti-inflammatory and neuroprotective effect of micronized and ultramicronized Palmitoylethanolamide (PEA). The aim of this study is to evaluate the effect of co-ultramicronized PEA and luteolin (700 mg + 70 mg in 10 ml) on the clinical outcomes of patients with acute ischemic stroke undergoing mechanical thrombectomy.
Trial Details
NCT Number NCT06777680
Lead Sponsor Ospedali Riuniti Trieste
Conditions Acute Ischemic Stroke AIS
Enrollment 60 participants
Start Date 2025-01
Primary Completion 2026-12 (estimated)
Study Completion 2026-12 (estimated)
Updated on ClinicalTrials.gov 2025-01-16