Heel pain: A systematic review.
Edward Kwame Agyekum, Kaiyu Ma
https://pubmed.ncbi.nlm.nih.gov/26643244Actively Recruiting
Led by Diskapi Teaching and Research Hospital · Updated on 2026-02-25
48
Participants Needed
1
Research Sites
17 weeks
Total Duration
Researchers are evaluating the outcomes of pulsed radiofrequency (PRF) treatment for patients with chronic plantar heel pain, a common condition often treated with interventional pain procedures. This observational study compares PRF applied only to the posterior tibial nerve versus PRF applied to both the posterior tibial and sural nerves. The study aims to understand whether targeting the sural nerve in addition to the posterior tibial nerve affects pain and function in these patients. The study includes patients who have already received ultrasound-guided PRF treatment as part of their routine clinical care. Two groups are compared: one received PRF only to the posterior tibial nerve, and the other received PRF to both the posterior tibial and sural nerves. No changes are made to treatment plans for study purposes, and patients are not randomized. Participants’ pain levels and foot function are assessed using the Visual Analog Scale (VAS) and the American Orthopaedic Foot and Ankle Society (AOFAS) hindfoot score. These assessments occur at baseline, 1 month, and 3 months after treatment. The study monitors these outcomes retrospectively to compare effectiveness between the two groups and includes patients aged 18 to 65 years with chronic heel pain and significant baseline pain.
CONDITIONS
Effect of Additional Sural Nerve PRF in Chronic Heel Pain
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 3 months
Participants who underwent pulsed radiofrequency treatment as part of routine clinical care are observed retrospectively. Pain intensity and functional outcomes are evaluated at baseline, 1 month, and 3 months after the procedure.
3 visits (baseline, 1 month, and 3 months post-procedure)
Total: 1 location
1
Ayse Betul Acar
Ankara, Turkey (Türkiye), 06500
Actively Recruiting
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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