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A Clinical Study of Ultrasound-guided Transforaminal Outside-In Short-term Dorsal Root Ganglion Stimulation for Thoracic Postherpetic Neuralgia

A Clinical Study of Ultrasound-guided Transforaminal Outside-In Short-term Dorsal Root Ganglion Stimulation for Thoracic Postherpetic Neuralgia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500115205
Enrollment
Unknown
Registered
2025-12-23
Start date
2026-01-01
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

postherpetic neuralgia

Interventions

treatment group:Receive a single short-duration (2-week) dorsal root ganglion stimulation (DRGS) treatment while continuing oral pregabalin (150 mg, BID). After electrode implantation, the patient wil
Control Group:Continue oral pregabalin (150 mg, BID) for 14 weeks to complete the follow-up.

Sponsors

Shanghai East Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age>=18 years. 2. Persistent pain following healing of cutaneous lesions from thoracic-segment (T2-T11) herpes zoster. 3. Pain Numeric Rating Scale (NRS) score >= 4. 4. Ability to provide written informed consent for study participation, understand the study procedures, and adequately complete patient-reported questionnaires. 5. Tolerate oral pregabalin 150 mg twice daily during the medication washout/observation period, and have an Average Daily Pain Score (ADPS) >= 4 at the end of this period.

Exclusion criteria

Exclusion criteria: 1. Presence of local or systemic infection at the intended puncture site; 2. Coagulation dysfunction (INR > 1.4 or platelet count 10% at screening or uncontrolled blood glucose within the preceding 1 month; 5. Other severe pain, neurological disorders, or dermatological conditions unrelated to postherpetic neuralgia that may interfere with assessment; 6. Implanted electronic devices such as cardiac pacemakers; 7. Severe cardiac, hepatic, or renal insufficiency; 8. Uncontrolled severe psychiatric illness or cognitive impairment; 9. Pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
Weekly Average Daily Pain Score;

Secondary

MeasureTime frame
Weekly Average Daily Pain Score;Weekly Average Daily Pain Score (ADPS) Response Rate;Neuropathic Pain Scale(NPS);Pain Catastrophizing Scale,PCS;Hospital Anxiety and Depression Scale;Pittsburgh Sleep Quality Index;Patient Global Impression of Change (PGIC);Rescue medication;

Countries

China

Contacts

Public ContactLiao Lijun

Shanghai East Hospital

Liao@pan-support.com+86 138 1742 8913

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026