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The clinical study of intercostal nerve pulsed radiofrequency in postherpetic neuralgia

The clinical study of intercostal nerve pulsed radiofrequency in postherpetic neuralgia: A randomised controlled trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN25588650
Enrollment
96
Registered
2010-06-21
Start date
2008-02-22
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Postherpetic neuraglia (PHN) Nervous System Diseases Cranial nerve disorders in diseases classified elsewhere

Interventions

Patients were randomised to receive one of the following treatments, once a week for 3 weeks: 1. Pulsed radiofrequency (42 degree, 120 second) of the intercostal nerve (Thoracic 1 to T12 level) 2. Sh

Sponsors

Xinhua Hospital (China)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age greater than 60 years 2. PHN history is longer than 3 months 3. Pain on Visual Analogue Scale (VAS) >3 (0-10 VAS scale) 4. PHN affected nerve sectors were thoracic nerves from T1 to T12 level 5. Refractory to formal treatment such as antiepileptic medicine, antidepressants, opioids and physical treatments and epidural block

Exclusion criteria

Exclusion criteria: 1. Exclusion criteria included withdraws from the study 2. Poor effect, intolerant to the study 3. Uncooperative and unable to finish the self evaluation (VAS, QOL and SF-36) 4. Coagulation disturbances 5. Allergies to local anaesthetic 6. Malignancy

Design outcomes

Primary

MeasureTime frame
1. Visual Analogue Scale (VAS) score, measured at baseline, days 3, 7, 14, 30 and 60, 6 months and 1 year 2. Flare pain per day during days 3, 7, 14, 30, 60 and at 6 months 3. Neurometer CPT/C (Neurotron, Inc) to measure three fiber function 4. SF-36 at baseline, 2 months, 6 months and 1 year following-up

Secondary

MeasureTime frame
1. Need to PRF again or other invasive operation at 2 day, 6 month or 1 year following-up 2. Dosage of rescue drug consumed per week at the end of treatment and after 4 weeks follow-up - including Tramadol and/or acetaminophen - and the dosage of combined drug, anti-depressive drug (amitriptyline) 3. Presence, frequency and duration of adverse effects at 7, 14, 30, and 60 days

Countries

China

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 24, 2026