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NOT YET RECRUITING
NCT07681063
NA

Palmitoylethanolamide/Luteolin Supplementation in Older Adults Undergoing Cardiac Surgery

Sponsor: Fondazione IRCCS San Gerardo dei Tintori

View on ClinicalTrials.gov

Summary

Postoperative Cognitive Dysfunction (POCD) is a common complication after surgery, particularly among older adults. It is characterized by cognitive impairment, reduced functional independence, and decreased quality of life. Growing evidence suggests that neuroinflammation plays a relevant role in POCD development and persistence. Palmitoylethanolamide (PEA) is an endogenous lipid mediator involved in the regulation of neuroinflammatory processes through the modulation of non-neuronal cells, while luteolin is a flavonoid with well-known antioxidant properties. Under conditions of prolonged neuroinflammation, endogenous PEA levels may be insufficient to adequately counteract pro-inflammatory signaling, making exogenous administration necessary. In this context, exogenous micronized and ultramicronized PEA (mPEA and umPEA) supplementation has been shown to modulate cognitive and executive functions, working memory, language, and activities of daily living. Moreover, the combination of umPEA and luteolin (PEALut) may produce synergistic effects by modulating neuroinflammation and supporting neuronal function. This study aims to evaluate whether postoperative administration of co-ultramicronized PEA and luteolin (700 mg + 70 mg in 10 mL), added to standard of care, may contribute to the mitigation of POCD in older adults undergoing elective cardiac surgery, compared to standard care alone.

Official title: Palmitoylethanolamide/Luteolin for the Maintenance of Cognitive Performance in Older Adults Undergoing Cardiac Surgery

Key Details

Gender

All

Age Range

65 Years - Any

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2026-06

Completion Date

2028-06

Last Updated

2026-07-02

Healthy Volunteers

No

Interventions

DIETARY_SUPPLEMENT

co-ultramicronized Palmitoylethanolamide + Luteolin (700 mg + 70 mg in 10 ml)

Oral suspension, 10 ml twice daily (every 12 hours), starting within 24 hours post-surgery and for 3 months, in add-on to the Standard of Care

OTHER

Standard of Care

Standard of Care

Locations (1)

Fondazione IRCCS San Gerardo dei Tintori

Monza, Italy