High-Voltage Long-Duration Pulsed Radiofrequency Combined With Liposomal Bupivacaine Subcutaneous Block for Herpes Zoster-Associated Neuralgia

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age40-85
SponsorShirong Tan

About this trial

Research Objectives Background and Significance: Zoster-associated neuralgia (ZAN) refers to neuropathic pain experienced by herpes zoster (HZ) patients before, during, and after rash resolution, characterized by paroxysmal, lightning-like, or knife-like sensations. Postherpetic neuralgia (PHN), a common type of chronic pain, is often accompanied by physical-psychological impairments, social dysfunction, and anxiety-depression. While high-voltage long-term pulsed radiofrequency (HL-PRF) has become a conventional treatment for ZAN, it is limited by residual postoperative localized pain and suboptimal efficacy for refractory cases. Liposomal bupivacaine (LB), a sustained-release analgesic providing up to 72 hours of pain relief, offers potential for combined subcutaneous injection to enhance symptomatic control.

Study Process:

This clinical study focuses on evaluating the efficacy of HL-PRF combined with LB subcutaneous injection in treating ZAN. The trial will be conducted from December 16, 2024, to December 14, 2026, with an anticipated enrollment of 92 participants. Patients will be randomized into two groups:

HL-PRF group: Under CT-guided localization, high-voltage pulsed radiofrequency (HL-PRF) therapy was precisely delivered to the pathologically compromised dorsal root ganglion (DRG).

HL-PRF+LB group: HL-PRF treatment followed by LB subcutaneous injection at the painful lesion site 2 hours post-procedure.

Clinical data will be collected preoperatively, and inflammatory factors will be assessed on the first postoperative day. Follow-up evaluations via telephone will occur at 1 week, 1 month, 3 months, and 6 months postoperatively. By analyzing changes in observed indicators before and after treatment, this study aims to determine the clinical efficacy of combining HL-PRF with LB subcutaneous injection for ZAN.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Voluntarily provided written informed consent.

Inadequate response to pharmacological or other non-surgical therapies OR intolerable drug-related adverse effects.

Herpes zoster (HZ) lesions involving cranial/cervicocephalic, cervical, thoracic, or lumbar dermatomes.

Moderate-to-severe pain intensity, defined as a Numerical Rating Scale (NRS) score ≥4 at baseline.

Disqualifiers

Severe cardiovascular diseases or life-threatening arrhythmias (e.g., heart failure, third-degree atrioventricular block without pacemaker implantation).

Contraindications to minimally invasive interventions (e.g., coagulation disorders, active infections).

Allergy to local anesthetics or lipid emulsions; Severe dysfunction of vital organs (cardiac, pulmonary, hepatic, or renal) rendering the patient unfit for the procedure.

Severe endocrine disorders or long-term use of corticosteroids/immunosuppressive agents.

Trial design

Design model

Parallel

Treatments tested in this trial

  • High-Voltage Long-Duration Pulsed Radiofrequency plus Liposomal Bupivacaine group

    Drug

    High-Voltage Long-Duration Pulsed Radiofrequency Combined with Liposomal Bupivacaine Subcutaneous Block

  • High-Voltage Long-Duration Pulsed Radiofrequency

    Other intervention

    High-Voltage Long-Duration Pulsed Radiofrequency

Treatment groups

46 Participants
are divided into 2 treatment groups
Group A: HL-PRF+LB groupExperimental treatment 1 intervention
Group B: HL-PRF groupOther 1 intervention

Trial outcomes

Primary outcomes

1

NRS

0 indicates no pain,1-3 indicate mild pain,4-6 indicate moderate pain, 7-10indicate severe pain.

Time frame
Baseline and on days 1, 3, 7, 30, 90 ,180 post-interventions

Secondary outcomes

1

The Zoster Brief Pain Inventory

The instrument comprises two validated domains: pain intensity quantification and pain-related functional interference assessment. With higher composite scores (range: 0-20) indicating greater multidimensional health impairment.

Time frame
Baseline and on days 7, 30, 90 ,180 post-interventions
2

Pittsburgh Sleep Quality Index Scale

Pittsburgh Sleep Quality Index (PSQI) total score ranges from 0 to 20, with lower scores indicating better sleep quality, thereby assessing overall sleep status.

Time frame
Baseline and on days 7, 30, 90 ,180 post-interventions
3

Use of analgesics (tramadol, gabapentin, or pregabalin)

Analgesic consumption metrics, including frequency of use and morphine equivalent daily dose (MEDD), were recorded to evaluate longitudinal changes in pain intensity."

Time frame
Baseline and on days 7, 30, 90,180 post-interventions
4

Adverse event rate

Adverse events include: Surgery-related complications (e.g., pneumothorax, hematoma, wound infection); Complications associated with bupivacaine liposome subcutaneous block, such as: Cardiac adverse events (e.g., arrhythmias, hypotension); Local tissue toxicity (e.g., myonecrosis, neuropathy).

Time frame
Day 1 post-interventions

Other outcomes

Sponsors and contacts

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Shirong Tan

Lead sponsor

Zunyi Medical College

Sponsor institution