Clinical Trial

Effects of Percutaneous Neuromouldation of the Saphenous Nerve in Patients With Patellofemoral Pain

Study acronym: PNMSNPFP
Unknown
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Record status
This record was last updated July 17, 2024 (before its estimated May 31, 2025 completion). Its status may not reflect the trial's current state.
Summary
The knee is a common source of musculoskeletal pain, with patellofemoral pain (PFP) standing out due to its high prevalence. This pain, frequent in adolescents and athletes, significantly impacts the quality of life by hindering daily activities such as climbing stairs and sitting for extended periods. Percutaneous neuromodulation of the saphenous nerve (PNM) emerges as a promising therapeutic approach in physiotherapy to alleviate these symptoms. A randomized controlled clinical trial is proposed in adults with PFP. Participants will be divided into two groups: one will receive PNM of the saphenous nerve, while the other will be a control group receiving puncture without electrical stimulation. Pain, extension strength, and knee range of motion will be evaluated before and after the intervention using the AKPS scale. Three sessions will be conducted with specific intervals, and a follow-up assessment will be performed three months later.
Protocol Amendment History 1 change
critical Trial status changed: Not Yet Recruiting → Unknown 2026-08-02
Trial Details
NCT Number NCT06505382
Lead Sponsor University of Alcala
Conditions Patellofemoral Pain
Enrollment 24 participants
Start Date 2024-09-30
Primary Completion 2025-05-31 (estimated)
Study Completion 2025-06-30 (estimated)
Updated on ClinicalTrials.gov 2024-07-17