Palmitoylethanolamide Modulates Central Sensitisation and Neuroinflammation in Chronic Low Back Pain
- NCT ID
- NCT07772141
- Registry status
- Recruiting
- Study type
- Not specified in the registry data
- Phase
- Not applicable
- Sponsor
- Beni-Suef University
Overview
ClinicalTrials.gov lists this study as Recruiting.
Enrollment: 106 participants (Estimated).
What is being studied
No interventions are listed in the registry data.
Who may be eligible
- Ages
- Not specified in the registry data
- Sex
- Not specified in the registry data
- Healthy volunteers accepted
- No
ClinicalTrials.gov lists the following 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
Study locations
1 study location is listed.
Site recruitment status is not specified in the registry data for these locations.
Countries: Egypt
Sample of listed locations
- Beni Suef University Hospital — Banī Suwayf, Egypt — Site recruitment status not specified in the registry data
Study details
- Start date
- January 1, 2026
- Primary completion date
- June 1, 2027
- First posted
- August 19, 2026
Source and update information
- Source
- ClinicalTrials.gov
- NCT ID
- NCT07772141
- Registry last updated
- August 19, 2026
- QualifiedStudies registry data refreshed
- September 21, 2026
View NCT07772141 on ClinicalTrials.gov
Trial information can change. Confirm current study details with the study team or the registry.
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