Comparison Between the Efficacy of Ultrasound-guided Erector Spinae Plane Block and Conventional Treatment for Pain Management in Patients With Post-herpetic Neuralgia
1 other identifier
interventional
60
1 country
1
Brief Summary
The present study aims to evaluate the efficacy of ultrasound-guided erector spinae plane block with steroids to relieve pain in cases of post-herpetic neuralgia, patient satisfaction, and record any complications post-injection.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Aug 2025
Shorter than P25 for not_applicable
1 active site
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
Study Start
First participant enrolled
August 1, 2025
CompletedFirst Submitted
Initial submission to the registry
November 20, 2025
CompletedFirst Posted
Study publicly available on registry
December 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2026
CompletedDecember 1, 2025
November 1, 2025
6 months
November 20, 2025
November 20, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Evaluate the efficacy of ultrasound-guided erector spinae plane block with steroids to relieve pain in cases of post-herpetic neuralgia
by VAS score
6 weeks
Secondary Outcomes (2)
Patient satisfaction
6 weeks
Complications
6 weeks
Study Arms (2)
Injection group
EXPERIMENTALconventional group
NO INTERVENTIONInterventions
Eligibility Criteria
You may qualify if:
- Patients with post-herpetic neuralgia not responding to medical treatment.
You may not qualify if:
- \- 1- Patient refusal 2- Age less than 20 years or older than 70 years. 3- Systemic Infection. 4-Patients with dementia or other diseases that could have impaired their memory or cognitive function.
- Immunocompromised patients, severe osteoporosis, and uncontrolled diabetes mellitus.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Alexandria University
Alexandria, Aleexandria, 21523, Egypt
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, CARE PROVIDER
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 20, 2025
First Posted
December 1, 2025
Study Start
August 1, 2025
Primary Completion
February 1, 2026
Study Completion
March 1, 2026
Last Updated
December 1, 2025
Record last verified: 2025-11