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Efficacy of an Intraoperative Periradicular Application of Platelet Rich Fibrin (PRF) on the Intensity of Residual Post-surgical Neuropathic Pain After a Surgery for Disc Herniation

Study acronym: NeuroPRF
StatusRecruiting
PhasePhase 3
Started2022-02-23
View on ClinicalTrials.gov ↗

Amendment history

2026-06-05
minor
Study Status v3
Completion date2025-01→2028-01
2023-04-14
minor
Study Status v2
Re-verified, no change to tracked fields
2022-02-24
notable
Not Yet Recruiting→Recruiting Study Status, Contacts/Locations v1
Trial statusNot Yet Recruiting→Recruiting
Primary completion dateestimated 2022-01→confirmed 2022-02-23
Start dateestimated 2022-01→confirmed 2022-02-23
Study sitesdetails revised at 1 of 1 site
2022-01-18
minor
Original filing
The prevalence of post-surgical lumbar neuropathic radiculopathy is approximately 30%. Poor response to the treatments recommended for neuropathic pain, namely antidepressants and/or gabapentinoids, requires the development of new techniques to prevent this chronic pain. Certain well-tolerated techniques, such as the administration of plasma enriched with platelets and fibrin (PRF), are increasingly used in regenerative medicine for their anti-inflammatory and analgesic properties. Thus, a periradicular intraoperative application of PRF may have an analgesic effect on the intensity of residual postsurgical neuropathic pain after disc herniation surgery.
Trial Details
NCT Number NCT05196503
Lead Sponsor University Hospital, Strasbourg, France
Conditions Neuropathic Pain, Chronic Postsurgical Pain
Enrollment 60 participants
Start Date 2022-02-23
Primary Completion 2022-02-23 (estimated)
Study Completion 2028-01 (estimated)
Updated on ClinicalTrials.gov 2026-06-08