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Evaluating the effect of a new interventional method for Herpes Pain

A randomised controlled study on the efficacy of pulsed radio frequency of thoracic paravertebral nerves for pain management in thoracic post herpetic neuralgia and expression of MicroRNA-133b

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/03/012693
Enrollment
40
Registered
2018-03-21
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Patients With established diagnosis of thoracic PHN

Interventions

Intervention1: Pulsed Radiofrequency lesioning of Thoracic Paravertebral Nerve: Pulsed Radiofrequency lesionioning of the thoracic paravertebral nerves of affected thoracic dermatome and one level abo

Sponsors

University College of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients should have a diagnosis of PHN with evident hyperalgesia and allodynia confined to mid thoracic and lower thoracic dermatomes 2. Patients of PHN should have had pain for at least 4 weeks after healing of rash 3. Pain intensity >= 5 on 10cm visual analogue scale (VAS)

Exclusion criteria

Exclusion criteria: Exclusion criteria 1. Patients with history of neurological intervention for PHN 2. Evidence of other sources of pain that may confound the diagnosis 16 3. Known history of taking Pregabalin for the treatment of PHN in past 4 weeks 4. Patients with past history of myocardial infarction, diabetes mellitus, pancreatitis and vasculitis 5. Patients with recent history of surgery 6. Patients with evidence of severe renal impairment 7. Patients with history of alcohol consumption and smoking

Design outcomes

Primary

MeasureTime frame
Proportion of patients achieving a VAS score of less than 3/10 at varying intervals following pulsed radiofrequency lesioningTimepoint: at the end of 1st week, at the end of 2nd week, at the end of 4th week, at the end of 8th week and end of 12th week.

Secondary

MeasureTime frame
To assess pain intensity, quality of life and alteration in MicroRNA-133b expression.Timepoint: at baseline and at the end of 1st week, at the end of 2nd week, at the end of 4th week, at the end of 8th week and end of 12th week

Countries

India

Contacts

Public ContactAshok Kumar Saxena

University College of Medical Sciences

profashoksaxena@gmail.com9868399703

Outcome results

None listed

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