Actively Recruiting

Phase 2
All Genders
NCT06273462

Palmitoylethanolamide for Chronic Inflammatory Pain Conditions

Led by Navy Medical Center San Diego · Updated on 2024-08-15

80

Participants Needed

1

Research Sites

64 weeks

Total Duration

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AI-Summary

What this Trial Is About

The goal of this clinical trial is to evaluate if a supplement called palmitoylethanolamide (PEA) is effective in reducing the pain in patients with chronic inflammatory pain conditions. The main question the trial aims to answer is if PEA works better at treating a patients pain and improving their function better than a placebo. Participants will be divided into two equal groups and asked to take either PEA or a placebo for 8 weeks.

CONDITIONS

Official Title

Palmitoylethanolamide for Chronic Inflammatory Pain Conditions

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Chronic inflammatory pain lasting more than 3 months
  • Pain intensity of 5 or higher on a 10-point scale
  • Pain not improved by other conservative treatments such as rest, ice, compression, or oral medications
Not Eligible

You will not qualify if you...

  • Severe allergy to any specific food such as nuts, eggs, or soy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Naval Medical Center San Diego

San Diego, California, United States, 92118

Actively Recruiting

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Research Team

B

Brian McLean Pain Physician, MD

CONTACT

I

IRB Administrator

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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