Clin2
NCT06777680Possibly a fitNot yet recruiting

Pea and luteolin for recovery after a first stroke

Acute Ischemic Stroke AIS

Part of Brain & nervous system, Heart & circulation clinical trials.

This trial tests whether a combination of two natural substances, palmitoylethanolamide (PEA) and luteolin, can help people who are recovering from a severe first stroke. The treatment is taken by mouth and is meant to reduce inflammation in the brain after a clot is removed, with the goal of improving recovery.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
60 people
Ages
60 years and older
Study type
Interventional

Who can take part

  • You must be 60 years of age or older.
  • You must be having your first-ever stroke — no previous strokes or mini-strokes.
  • The stroke must be caused by a blockage in the middle cerebral artery, confirmed by imaging (angio-CT and CTP).
  • You must be eligible for mechanical thrombectomy (a procedure to remove the clot) within the guideline-approved time window.
  • Your stroke must be severe enough (NIHSS score greater than 6).
  • You must not have certain other conditions, such as dementia, Parkinson's, psychiatric disorders, chronic inflammatory diseases, active cancer, or severe swallowing problems.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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