Pulsed Radiofrequency in Post Herptic Neuralgia
Efficacy and Safety of STP Pulsed Radiofrequency Versus Regular Pulsed Radiofrequency for Treatment of Post Herpetic Neuralgia
1 other identifier
interventional
100
1 country
2
Brief Summary
Comparing between regular pulsed Radiofrequency and irregular pulsed Radiofrequency for treatment of postherpetic neuralgia
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Oct 2025
Shorter than P25 for not_applicable
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 27, 2025
CompletedStudy Start
First participant enrolled
October 1, 2025
CompletedFirst Posted
Study publicly available on registry
October 6, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 31, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
March 31, 2026
CompletedOctober 6, 2025
February 1, 2025
6 months
September 27, 2025
September 27, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Pain level by Numerical Rating Scale
One day , One week , One month ,Three months postprocedure.
Study Arms (2)
Irregular pulsed Radiofrequency treatment (STP)
ACTIVE COMPARATORRegular pulsed Radiofrequency treatment
ACTIVE COMPARATORInterventions
Flouroscopic guided irregular pulsed Radiofrequency (STP) for dorsal root ganglion
Fluoroscopic guided regular pulsed Radiofrequency for the dorsal root ganglion
Eligibility Criteria
You may qualify if:
- Patients with Herps Zoster neuralgia lasting more than one month Neck thoracic lumbar ganglion involvement Refractory to conventional therapy
You may not qualify if:
- Infection ,tumour at the puncture site Severe cardiovascular or cerebrovascular disease Liver, kidney dysfunction Abnormal coagulation Uncontrolled DM Psychatric diseases Patient refusal
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Sohag Universitylead
Study Sites (2)
Medical research ethics committee
Sohag, Sohag Governorate, 82511, Egypt
Medical research ethics committee
Sohag, Egypt
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Lecturer of anaesthesia and pain management
Study Record Dates
First Submitted
September 27, 2025
First Posted
October 6, 2025
Study Start
October 1, 2025
Primary Completion
March 31, 2026
Study Completion
March 31, 2026
Last Updated
October 6, 2025
Record last verified: 2025-02
Data Sharing
- IPD Sharing
- Will not share