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Recruiting NCT07772141

NCT07772141 Palmitoylethanolamide Modulates Central Sensitisation and Neuroinflammation in Chronic Low Back Pain

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Clinical Trial Summary
NCT ID NCT07772141
Status Recruiting
Phase —
Sponsor Beni-Suef University
Condition Chronic Low-back Pain
Study Type INTERVENTIONAL
Enrollment 106 participants
Start Date 2026-01-01
Primary Completion 2027-06-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 65 Years
Study Type INTERVENTIONAL
Interventions
Palmitoylethanolamide

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 106 participants in total. It began in 2026-01-01 with a primary completion date of 2027-06-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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

Inclusion Criteria: * 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. * ASA I and ASA II Exclusion Criteria: * Neurological disorders * psychiatric illness * pregnancy * prior spinal surgery * concurrent use of immunomodulatory drugs * contraindications to TMS. * Allergy to the drug

Contact & Investigator

Central Contact

Hager Essam Nasrallah

✉ hagernasrallah778@gmail.com

📞 +201149106597

Principal Investigator

Hatem Elmoutaz Mahmoud, M.D

STUDY CHAIR

Professor of Anaesthesiology,Surgical intensive care and pain management,Faculty of medicine

Frequently Asked Questions

Who can join the NCT07772141 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 65 Years, studying Chronic Low-back Pain. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07772141 currently recruiting?

Yes, NCT07772141 is actively recruiting participants. Contact the research team at hagernasrallah778@gmail.com for enrollment information.

Where is the NCT07772141 trial being conducted?

This trial is being conducted at Banī Suwayf, Egypt.

Who is sponsoring the NCT07772141 clinical trial?

NCT07772141 is sponsored by Beni-Suef University. The principal investigator is Hatem Elmoutaz Mahmoud, M.D at Professor of Anaesthesiology,Surgical intensive care and pain management,Faculty of medicine. The trial plans to enroll 106 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology