Research study · Frontiers in Nutrition · 2025
Fixed combination of palmitoylethanolamide and melatonin in preventive therapy of migraine: results from a randomized clinical trial
Verified on PubMed Oxford CEBM Level 1B: Randomized Controlled Trial
A 2025 randomized controlled trial in Frontiers in Nutrition tested palmitoylethanolamide in migraine. It helped in this small study, and no side effects were reported. This study suggests that a palmitoylethanolamide and melatonin supplement may reduce migraine frequency and severity in people with occasional migraines, but it involved only 60 people followed for three months.
In plain language
Study overview
This study looked at whether a nightly supplement combining a natural fatty compound called palmitoylethanolamide with the sleep hormone melatonin could help people who get occasional migraines. Sixty adults were split evenly into two groups, and neither the participants nor the researchers knew who was getting the real supplement or the dummy pill.
Findings
It helped in this small study, and no side effects were reported. Over three months, people taking the supplement had fewer migraine days, shorter and milder attacks, and less disability than those taking the dummy pill.
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The deeper readScientific analysis
Introduction: Migraines are neurological disorders which significantly impact quality of life. Current pharmacological treatments often have adverse effects, prompting the search for alternatives with fewer side effects. Several studies have described the antimigraine properties of palmitoylethanolamide (PEA) and melatonin. Materials and methods: The efficacy of the association of hydrodispersible PEA (1,200 mg) and melatonin (0.2 mg) was assessed by a randomized, three-month, double-blind, placebo-controlled trial (PEATONIDE; n = 30 patients; placebo; n = 30 patients). The primary outcome was the reduction of migraine frequency, while secondary outcomes included the reduction of intensity, duration, and grade of disability, assessed by a self-reported daily headache diary. Results: The formulation displayed a significant reduction in frequency (T3 months: 2.2 ± 0.4 MMDs; T0 baseline: 3.4 ± 0.5 MMDs, p < 0.001 vs baseline T0) and duration, intensity, disability, and incidence of associated symptoms after 3 months of treatment. No adverse effects were observed during the treatment. Conclusion: These findings suggest that PEATONIDE may be a promising adjunctive approach for migraine management. However, given the relatively small sample size, further large-scale and multicenter trials are needed to confirm its clinical applicability in broader migraine population.
The paper
Citation
Piccolo V, Marzocchi A, Maisto M, Summa V, Tenore GC, Amoresano A Fixed combination of palmitoylethanolamide and melatonin in preventive therapy of migraine: results from a randomized clinical trial. Frontiers in Nutrition (2025). PubMed 40276532 · DOI
Limitations the authors noted
Small sample of 60 patients, with only 16 participants (8 per arm) having aura. Population limited to low-frequency episodic migraine; high-frequency episodic and chronic migraine not studied. Reliance on self-reported diaries and lifestyle data without objective monitoring. Per-protocol analysis reported; intention-to-treat not explicitly stated. Authors report no attrition, yet the CONSORT diagram and recruitment numbers (70 recruited, 10 ineligible) warrant verification. Concomitant analgesic use (acetaminophen, NSAIDs) permitted during attacks. Single-country, single-center recruitment; no sex-stratified analysis. Funding not declared; unclear whether the product (PEATONIDE, a patented combination) was supplied or developed by any party with commercial interest.
In practice
Why this matters
This study suggests that a palmitoylethanolamide and melatonin supplement may reduce migraine frequency and severity in people with occasional migraines, but it involved only 60 people followed for three months. It does not show the supplement works for people with frequent or chronic migraine, for people with migraine aura, or over longer periods. A reader should treat it as an early, encouraging signal that calls for larger, independent trials rather than as proof of benefit.
Frequently asked questions
Clinical Questions & Answers
What were the primary clinical findings regarding Palmitoylethanolamide and Adverse events?
It helped in this small study, and no side effects were reported. Over three months, people taking the supplement had fewer migraine days, shorter and milder attacks, and less disability than those taking the dummy pill.
What study limitations or clinical safeguards should patients keep in mind?
Small sample of 60 patients, with only 16 participants (8 per arm) having aura. Population limited to low-frequency episodic migraine; high-frequency episodic and chronic migraine not studied. Reliance on self-reported diaries and lifestyle data without objective monitoring.
Browse related research
Condition: Adverse events Condition: Insomnia Condition: Migraine Topic: Palmitoylethanolamide
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Reviewed by Dr. Caplan on October 24, 2026.
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