Cycle-length evidence
PEA cycle length: what human studies ran
Not approved — research use onlyAHuman trial evidence
Short answer: there is no established PEA cycle length or break. The human studies below ran for set periods under monitoring; none tested repeated courses.
Treatment and follow-up in human studies
What has not been tested
- On-and-off schedules or breaks between courses.
- Repeated courses and long-term exposure beyond the periods listed.
- PEA combined with other compounds, unless a study above says so.
Frequently asked questions
Is there an established PEA cycle length?
No. Human studies administered PEA for the periods listed on this page. Those are study durations; none tested an on-and-off schedule or a break.
What is the longest human study of PEA?
The durations are listed on this page with their sources; compare them directly rather than relying on a summary.
Do study durations tell me how long to use something?
No. A study duration is how long investigators administered a compound to selected participants under monitoring. It is not a recommended course, and a break between courses has not been tested for any compound on this site that is not approved.
References
- The pharmacology of palmitoylethanolamide and first data on the therapeutic efficacy of some of its new formulations Br J Pharmacol. 2017
- Palmitoylethanolamide in the Treatment of Chronic Pain: A Systematic Review and Meta-Analysis of Double-Blind Randomized Controlled Trials Nutrients. 2023
- The nuclear receptor peroxisome proliferator-activated receptor-alpha mediates the anti-inflammatory actions of palmitoylethanolamide Mol Pharmacol. 2005
- Palmitoylethanolamide supplementation for human health: A state-of-the-art systematic review of Randomized Controlled Trials in patient populations Brain Behav Immun Health. 2025
- Meta-Analysis of Palmitoylethanolamide in Pain Management: Addressing Literature Gaps and Enhancing Understanding Nutr Rev. 2025
- Efficacy, safety, and tolerability of palmitoylethanolamide in the management of diabetic neuropathic pain: a systematic review and meta-analysis J Diabetes Metab Disord. 2026
- The Effect of Palmitoylethanolamide on Pain Intensity, Central and Peripheral Sensitization, and Pain Modulation in Healthy Volunteers - A Randomized, Double-Blinded, Placebo-Controlled Crossover Trial Nutrients. 2022
- Palmitoylethanolamide Does Not Affect Recovery from Exercise-Induced Muscle Damage in Healthy Males Med Sci Sports Exerc. 2024
- Palmitoylethanolamide (Levagen+) for acute menstrual pain: a randomized, crossover, double-blind, placebo-controlled trial Women Health. 2025
- Targeting PTSD with ultramicronized palmitoylethanolamide: Results from a randomized trial integrating pharmacotherapy and cognitive behavioral therapy J Psychiatr Res. 2026
- Palmitoylethanolamide counteracts substance P-induced mast cell activation in vitro by stimulating diacylglycerol lipase activity J Neuroinflammation. 2019
- Pharmacokinetics of micronized and water dispersible palmitoylethanolamide in comparison with standard palmitoylethanolamide following single oral administration in male Sprague-Dawley rats Indian J Pharmacol. 2025
- PubChem compound record for palmitoylethanolamide (CID 4671; N-(2-hydroxyethyl)hexadecanamide, CAS 544-31-0) PubChem. 2026
- Drugs@FDA application data queried through openFDA for palmitoylethanolamide and palmidrol (no matching application record returned on 22 October 2026) openFDA / Drugs@FDA. 2026
- Dietary Supplement Label Database (DSLD) search for palmitoylethanolamide, returning 718 US dietary supplement labels on 22 October 2026 NIH Office of Dietary Supplements. 2026
- International Standard: Prohibited List 2026 (full-document search for palmitoylethanolamide and ethanolamide returned no named entry) World Anti-Doping Agency. 2026
- A Randomized, Double-Blind, Placebo-Controlled, Multicenter Phase IIA Study of FSD201 (Ultramicronized PEA) + Standard of Care Vs SOC in the Treatment of Hospitalized Patients With COVID-19 (NCT04619706; terminated) ClinicalTrials.gov. 2022
- Bulk Drug Substances Nominated for Use in Compounding Under Section 503A of the FD&C Act (updated May 14, 2026; palmitoylethanolamide not listed in categories 1, 2 or 3) FDA. 2026
- A double-blind randomized placebo controlled study assessing safety, tolerability and efficacy of palmitoylethanolamide for symptoms of knee osteoarthritis Inflammopharmacology. 2019
- A randomized controlled trial assessing the safety and efficacy of palmitoylethanolamide for treating diabetic-related peripheral neuropathic pain Inflammopharmacology. 2022
- Ultramicronized palmitoylethanolamide in spinal cord injury neuropathic pain: a randomized, double-blind, placebo-controlled trial Pain. 2016
- Palmitoylethanolamide as adjunctive therapy in major depressive disorder: A double-blind, randomized and placebo-controlled trial J Affect Disord. 2018
- Palmitoylethanolamide as adjunctive therapy for autism: Efficacy and safety results from a randomized controlled trial J Psychiatr Res. 2018
- Efficacy and safety of palmitoylethanolamide as an adjunctive treatment for acute mania: A randomized, double-blind, placebo-controlled trial Psychiatry Clin Neurosci. 2022
- Palmitoylethanolamide Reduces Proinflammatory Markers in Unvaccinated Adults Recently Diagnosed with COVID-19: A Randomized Controlled Trial J Nutr. 2022
- The Efficacy of Palmitoylethanolamide (Levagen+) on the Incidence and Symptoms of Upper Respiratory Tract Infection - A Double Blind, Randomised, Placebo-Controlled Trial Nutrients. 2023