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临床试验/NCT07596823
NCT07596823招募中不适用

Hematological Inflammatory Indices as Predictors of Treatment Response to Sympathetic Nerve Blocks in Neuropathic Pain: A Prospective Observational Study

Ankara City Hospital Bilkent1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2026年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
120
试验地点
1

研究概览

简要总结

This prospective observational study aims to evaluate the relationship between hematological inflammatory indices and clinical treatment response in patients with neuropathic pain undergoing sympathetic nerve block procedures as part of routine clinical care. Hematological parameters including neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), monocyte-to-lymphocyte ratio (MLR), systemic immune-inflammation index (SII), systemic inflammation response index (SIRI), aggregate index of systemic inflammation (AISI), and red cell distribution width (RDW) will be evaluated before and after treatment. The association between changes in these indices and pain outcomes will be analyzed.

详细描述

Neuropathic pain is a complex chronic pain condition involving inflammatory, neural, and immune-mediated mechanisms. Increasing evidence suggests that systemic inflammatory processes may contribute to the pathophysiology and persistence of neuropathic pain. Hematological inflammatory indices derived from routine complete blood count parameters have recently emerged as inexpensive and accessible biomarkers reflecting systemic inflammatory status.

Although several studies have investigated inflammatory markers in chronic pain syndromes, data regarding the relationship between hematological inflammatory indices and treatment response following sympathetic nerve block interventions in neuropathic pain are limited.

This prospective observational study aims to evaluate whether hematological inflammatory indices are associated with treatment outcomes in neuropathic pain patients treated with sympathetic nerve block procedures as part of routine clinical management. Adult patients diagnosed with neuropathic pain and scheduled for sympathetic nerve block treatment will be prospectively followed for 3 months.

Clinical outcomes including Numeric Rating Scale (NRS), DN4 and/or LANSS neuropathic pain scores, Global Perceived Effect (GPE), and analgesic consumption will be recorded. Hematological indices including NLR, PLR, MLR, SII, SIRI, AISI, and RDW will be calculated using routine hemogram parameters.

The study is designed as a non-interventional, single-center, prospective observational clinical study. The treatment approach will not be altered for research purposes.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age ≥18 years
  • Diagnosis of neuropathic pain based on clinical evaluation
  • DN4 and/or LANSS scores compatible with neuropathic pain
  • Undergoing sympathetic nerve block as part of routine clinical treatment
  • Availability of pre-treatment and follow-up hemogram parameters
  • Ability to provide written informed consent

排除标准

  • Age <18 years
  • Active infection or acute inflammatory disease
  • Active malignancy
  • History of hematological disease
  • Immunosuppressive therapy or systemic corticosteroid use
  • Major surgery or severe trauma within the last month
  • Pregnancy or breastfeeding
  • Autoimmune or rheumatologic inflammatory disease
  • Missing follow-up data

研究组 & 干预措施

Neuropathic Pain Cohort

Adult patients diagnosed with neuropathic pain undergoing sympathetic nerve block procedures as part of routine clinical care in the Algology Clinic of Ankara Bilkent City Hospital.

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ülkü Sabuncu

Assoc Prof

Ankara City Hospital Bilkent

研究点 (1)

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