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

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorUniversity of Alcala

About this trial

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.

Eligibility criteria

Qualifiers

Be 18 years or older.

Knee pain in the anterior aspect or around the patella for at least 1 month, exacerbated by activities such as squatting, stair climbing, or prolonged sitting.

Patients experiencing difficulty participating in sports due to pain.

Disqualifiers

Previous surgical intervention on the painful knee.

Previous diagnosed knee pathology.

Recent trauma or acute injury to the knee that may have led to the development of pain.

Antiplatelet or anticoagulant therapy.

Trial design

Treatments tested in this trial

  • Ultrasound-guided percutaneous neuromodulation

Treatment groups

24 Participants
are divided into 2 treatment groups

Sponsors and collaborators