Actively Recruiting
Which Is More Effective in the Treatment of Postherpetic Neuralgia: Erector Spinae Plane Block or Transcutaneous Radiofrequency?
Led by Diskapi Teaching and Research Hospital · Updated on 2026-02-25
50
Participants Needed
1
Research Sites
17 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This observational study compares two treatments for postherpetic neuralgia, a difficult type of nerve pain that affects quality of life. Researchers aim to evaluate the pain relief and neuropathic pain features in patients who have received either ultrasound-guided erector spinae plane (ESP) block or transcutaneous radiofrequency (RF) treatment. The study uses pain scores from the Visual Analog Scale (VAS) and the Self-Leeds Assessment of Neuropathic Symptoms and Signs (S-LANSS) to measure outcomes. Patients included in this study have already undergone one of the two treatments as part of their routine care at the Algology Clinic. The ESP block involves injecting a combination of dexamethasone, bupivacaine, and saline near the affected nerves using ultrasound guidance. The RF treatment uses adhesive electrodes to deliver pulsed electrical stimulation to the painful area for two weekly sessions. No changes were made to patients' treatment plans for this research. Researchers will review patients' pain scores before treatment, immediately after, and one month later to compare the two groups. The study looks at how well each treatment reduces pain and neuropathic symptoms at these time points. Participants' medical records and pain assessments are used for this retrospective evaluation. The study runs from June 2025 to October 2026 and includes adults aged 18 to 80 years with postherpetic neuralgia.
CONDITIONS
Brief Title
Erector Spinae Plane Block Versus Transcutaneous Radiofrequency in Postherpetic Neuralgia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of postherpetic neuralgia involving cervical, thoracic, or lumbar regions
- Age between 18 and 80 years
- Persistent pain despite conservative treatment
- Baseline VAS score > 5
You will not qualify if you...
- Ophthalmic or extremity postherpetic neuralgia
- Allergy to local anesthetics
- 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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 2 weeks
Participants who underwent either ultrasound-guided erector spinae plane block or transcutaneous radiofrequency therapy as part of routine clinical care are observed for treatment outcomes.
1 procedure visit for erector spinae plane block or 2 weekly visits for transcutaneous radiofrequency treatment
Duration - 1 month
Participants are evaluated for treatment outcomes using pain and sensory assessments at 1 month after treatment.
1 follow-up visit (in-person)
Trial Site Locations
Total: 1 location
1
Ayse Betul Acar
Ankara, Turkey (Türkiye), 06500
Actively Recruiting
Research Team
A
AYSE BETUL ACAR
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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