Ireland
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Recruiting Not applicable

Predicting Ultrasound-Guided Thoracic PVB Success in Herpetic Neuralgia

NCT06761924 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2025-02
Last updated
2025-01-07

Condition(s) studied

Patient Satisfaction

Investigational drug(s) / intervention(s)

Ultrasound-Guided Thoracic Paravertebral nerve blockUltrasound-Guided Thoracic Paravertebral nerve block

Ultrasound-Guided Thoracic Paravertebral nerve block: The patients will receive ultrasound-guided TPVB with 25 mg bupivacaine 0.5%, plus 8 mg dexamethasone (10 mL volume)

Ultrasound-Guided Thoracic Paravertebral nerve block: ultrasound-guided TPVB with 10 mL of saline without knowing which treatment they are receiving, maintaining blinding throughout the study.

Study summary

This study aims to fill the knowledge gap by investigating the predictors of success for TPVB in patients with herpetic neuralgia. By identifying demographic, clinical, previous medications and procedural factors associated with positive outcomes, this research seeks to enhance the efficacy of TPVB and improve pain management strategies for patients suffering from herpetic neuralgia.

Eligibility

Sex
ALL
Min age
18 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria: * Adults aged from18 to 70 years * Diagnosed with herpetic neuralgia. * Able and willing to provide informed consent. * ASA I - II * One dermatomal affection * Thoracic distribution Exclusion Criteria: * Contraindications to TPVB as ( Infection at site of injection, empyema , coagulopathy and neoplastic lesion occupying the paravertebral space) * Known allergies to study medications (bupivacaine, Dexamethasone). * Severe comorbidities that could interfere with study participation.

Primary outcome measure(s)

  • The Numeric Pain Rating Scale (NRS) — baseline , 24 hours , 2 weeks ,6 weeks , 3 months and 6 months post- intervention
    The patient is asked to make three pain ratings, corresponding to current, best and worst pain experienced over the past 24 hours. The average of the 3 ratings was used to represent the patient's level of pain over the previous 24 hours

Trial sites (1)

FacilityCityRegionStatus
Beni Suef University Hospital Banī Suwayf Beni Suweif Governorate Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06761924 on ClinicalTrials.gov ↗ ← All trials in Egypt