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Ultrasound-Guided Thoracic Paravertebral Injection of Platelet-Rich Plasma for the Treatment of Thoracic Herpes Zoster-Related Pain: A Prospective, Randomized Controlled, Open-Label, Endpoint-Blind, Single-Center Study

Ultrasound-Guided Thoracic Paravertebral Injection of Platelet-Rich Plasma for the Treatment of Thoracic Herpes Zoster-Related Pain: A Prospective, Randomized Controlled, Open-Label, Endpoint-Blind, Single-Center Study

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087248
Enrollment
Unknown
Registered
2024-07-23
Start date
2024-08-01
Completion date
Unknown
Last updated
2025-12-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Herpes zoster

Interventions

Control Group:Standard Antiviral Therapy
Intervention Group:Ultrasound-Guided Thoracic Paravertebral PRP Injection Therapy

Sponsors

The Second Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1.Diagnosed with herpes zoster involving unilateral thoracic nerves (T1-T12); 2. Age = 50 years and disease duration = 2 week; 3. Mean average pain intensity score (11-point NRS) within 24 hours before randomization = 4 points; 4. Agree to participate in this study and be able to sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with disseminated herpes zoster or combined with herpes zoster at other locations; 2. Coagulation dysfunction, taking anticoagulant drugs or/and antiplatelet drugs; 3. Systemic infections or infection at the puncture site; 4. Pregnant or lactating women; 5. Patients with immunodeficiency diseases, severe cardiovascular, cerebrovascular, and respiratory diseases, or other serious systemic diseases that prevent cooperation with the treatment; 6. Patients with mental illness; 7. Patients with thoracic spine deformity or a history of thoracic spine surgery that affects ultrasound positioning; 8. Patients who have contraindications for PRP or are allergic to treatment-related drugs such as famciclovir, gabapentin, pregabalin, Nonsteroidal Antiinflammatory Drugs(NSAIDs), and tramadol; 9. Patients with a recent history of other pain management treatments;

Design outcomes

Primary

MeasureTime frame
Incidence Rate of Postherpetic Neuralgia (PHN);

Secondary

MeasureTime frame
Pain characteristics;Skin lesion recovery;Quality of life score;Sleep quality;consumption and name of rescue analgesics;Pain intensity;Adverse events and safety assessment;

Countries

China

Contacts

Public ContactZongbin Jiang

The Second Affiliated Hospital of Guangxi Medical University

2010pain@163.com+86 771 324 4390

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 5, 2026