Palmitoylethanolamide Modulates Central Sensitisation and Neuroinflammation in Chronic Low Back Pain

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorBeni-Suef University

About this trial

Low back pain (LBP) is a public and occupational health problem that is a major professional, economic and social burden. Up to 84% of the general population will experience an episode of LBP during its life time, and recurrence rates are high. Acute LBP is the second reason for consultations in general medicine, and chronic LBP is the eighth. One in five LBP episodes result in sick leave. LBP represents 30% of sick leaves that are longer than 6 months, and 20% of work accidents. LBP has become the leading cause of exclusion from work before the age of 45, and the third cause of work disabilities in France.

In 2020 globally, LBP affected approximately 619 million people, making it the leading cause of disability worldwide. This number is projected to rise to 843 million by 2050, driven by population growth and aging.

Eligibility criteria

Qualifiers

With chronic pain (more than 3 months)

Patients with NRS (4 -7)

MRI evidence of disc protrusion or prolapse limited to one or two lumbar discs, without extensive multi-level pathology

Diagnosed clinically with low back pain due to disc disease.

Disqualifiers

Neurological disorders

psychiatric illness

pregnancy

prior spinal surgery

Trial design

Treatments tested in this trial

  • Palmitoylethanolamide

Treatment groups

106 Participants
are divided into 2 treatment groups

Sponsors and collaborators