Effectiveness of Ultrasonography-Guided Serratus Posterior Superior Intercostal Plane Block in Thoracic Postherpetic Neuralgia: A Retrospective Cohort Study
pain
1 other identifier
observational
34
1 country
1
Brief Summary
Postherpetic neuralgia (PHN) is a chronic pain syndrome that can be resistant to treatment, leading to physical and social disability, psychological disturbances, and potentially persisting for years . The varicella-zoster virus remains latent in the sensory neurons of individuals who have previously contracted varicella (chickenpox). Reactivation of the latent virus results in herpes zoster (HZ). In most patients, HZ initially presents with dermatomal pain, and within a few days, characteristic dermatomal vesicular eruptions typically develop. These skin lesions usually heal within 2-4 weeks; however, pain may persist even after the resolution of the rash . The pathogenesis of PHN involves increased sensitization of central neurons, decreased function of inhibitory neuronal pathways, inflammation and nerve injury within the peripheral nervous system, and abnormal signal transmission following such damage. PHN represents the most common complication of HZ. It occurs in approximately 9-19% of all patients with HZ. The incidence of PHN increases with advancing age: it affects approximately 2% of individuals younger than 50 years, about 20% of those older than 50 years, and nearly 35% of those older than 80 years . Various treatment modalities, including pharmacologic agents and interventional procedures, are available for the management of PHN-related pain. This study primarily aims to evaluate the change in pain in PHN patients who underwent SPSIPB using the NRS-11. The secondary aim was to evaluate the effect of SPSIPB on neuropathic pain characteristics using the DN-4 scale and to investigate its effects on patients' quality of life using SF-12 scale.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Jul 2025
Shorter than P25 for all trials
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
July 1, 2025
CompletedFirst Submitted
Initial submission to the registry
July 6, 2025
CompletedFirst Posted
Study publicly available on registry
July 16, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
September 15, 2025
CompletedDecember 12, 2025
December 1, 2025
1 month
July 6, 2025
December 5, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Numeric Rating Scale -11 (NRS-11)
It is an 11-point scale used to describe pain. It is based solely on the patient's ability to perform activities of daily living and can be used for adults and children ages 10 and older.
3 months
Secondary Outcomes (2)
Douleur Neuropathique en 4 Questions(DN4)
3 months
Short Form- 12
3 months
Study Arms (1)
Effectiveness of Ultrasonography-Guided Serratus Posterior Superior Intercostal Plane Block in Thora
Eligibility Criteria
Patients over 18 years of age who underwent a single-session ultrasound (US )guided serratus posterior superior intercostal plane block (SPSIPB) in the thoracic region (T1-T10 dermatomes) for PHN between June 2023 and February 2025 were evaluated. SPSIPB was performed in patients whose complaints persisted despite existing medical treatments.
You may qualify if:
- Patients over 18 years of age
- \- who underwent a single-session ultrasound (US)-guided serratus posterior superior intercostal plane block (SPSIPB) in the thoracic region (T1-T10 dermatomes) for PHN between June 2023 and February 2025 were evaluated. -SPSIPB was performed in patients whose complaints persisted despite existing medical treatments.
You may not qualify if:
- congenital anomalies of the spine; neck pain accompanied by neurological deficits
- pregnancy
- mental or psychotic disorders
- hematologic diseases causing bleeding or coagulation disorders
- use of antiplatelet or anticoagulant drugs or other medications predisposing to bleeding
- severe systemic infections such as sepsis
- local infection at the planned intervention site
- known allergy to any of the drugs to be used; or a history of invasive procedures for PHN in the thoracic region within the past three months.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
İKanuni Sultan Süleyman Training and Research Hospital
Küçükçekmece, Istanbul, (507) 277-4773, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
halil ibrahim altun
Kanuni Sultan Süleyman Training and Research Hospital
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- pain specialist
Study Record Dates
First Submitted
July 6, 2025
First Posted
July 16, 2025
Study Start
July 1, 2025
Primary Completion
August 1, 2025
Study Completion
September 15, 2025
Last Updated
December 12, 2025
Record last verified: 2025-12