Palmitoylethanolamide is effective for chronic pain, but the optimal duration of its micron-size treatment is undefined.
Micron-size Palmitoylethanolamide for 60+ days significantly reduces chronic pain, an indispensable option for managing chronic pain.
Palmitoylethanolamide is effective for chronic pain, but the optimal duration of its micron-size treatment is undefined. This systematic review and meta-analysis assessed the potential benefits of extended (>60 days) versus shorter-duration Palmitoylethanolamide therapy in relieving chronic pain.
A comprehensive literature search was conducted across scientific databases to recognise clinical trials fulfilling criteria where micron-size Palmitoylethanolamide was administered for at least 60 days. The Visual Analogue Scale (VAS) or Numeric Rating Scale (NRS) were used to assess pain. Nine studies involving 742 patients met the inclusion criteria. A meta-analysis was performed to compare pain intensity reductions between treatment durations.
The meta-analysis demonstrated a considerable reduction in pain intensity with 60 days of micron-size Palmitoylethanolamide supplementation compared to 30 days (1.36 points reduction, p < 0.01). Secondary analysis revealed a 2.08-point decrease in NRS/VAS scores during the first month, equating to a 35.1% reduction in pain intensity. This improvement continued with an additional 35.4% decrease in the second month of treatment (Table 1):
Extended supplementation of micron-size Palmitoylethanolamide provides a significant advantage over shorter treatments, particularly for patients experiencing incomplete pain management.
Nutrients
Extended Treatment with Micron-Size Oral Palmitoylethanolamide (PEA) in Chronic Pain: A Systematic Review and Meta-Analysis
Vittorio Schweiger et. al.
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