Actively Recruiting

Age: 18Years - 65Years
All Genders
ID07383558

Does Targeting the Sural Nerve Along with the Posterior Tibial Nerve Increase Effectiveness of Pulsed Radiofrequency Treatment in Chronic Plantar Heel Pain?

Led by Diskapi Teaching and Research Hospital · Updated on 2026-02-25

48

Participants Needed

1

Research Sites

17 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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

Brief Title

Effect of Additional Sural Nerve PRF in Chronic Heel Pain

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 65 years
  • Presence of chronic plantar heel pain
  • Baseline Visual Analog Scale (VAS) score greater than 5
Not Eligible

You will not qualify if you...

  • History of foot fracture or tumor
  • Pregnancy
  • Coagulopathy or use of antiplatelet therapy
  • Cognitive impairment preventing informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Monitoring

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)

Trial Site Locations

Total: 1 location

1

Ayse Betul Acar

Ankara, Turkey (Türkiye), 06500

Actively Recruiting

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How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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Published Research Related To This Trial

Ultrasound-Guided Pulsed Radiofrequency Stimulation of Posterior Tibial Nerve: A Potential Novel Intervention for Recalcitrant Plantar Fasciitis.

Yung-Tsan Wu, Chih-Ya Chang, Yu-Ching Chou...

https://pubmed.ncbi.nlm.nih.gov/28209507

Comparison of tibial nerve pulsed radiofrequency and intralesional radiofrequency thermocoagulation in the treatment of painful calcaneal spur and plantar fasciitis: a randomized clinical trial.

Gokhan Yildiz, Gevher Rabia Genc Perdecioglu, Damla Yuruk...

https://pubmed.ncbi.nlm.nih.gov/38652568