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临床试验/NCT02383524
NCT02383524Unknown不适用

Does the Brain-derived Neurotrophic Factor Val66Met Gene Polymorphism Predict Inter-individual Variation in Responsiveness Following Lumbar Radiofrequency Denervation? A Single-centre, Prospective, Exploratory Study in Subjects Diagnosed With Zygapophysial Joint Pain

Guy's and St Thomas' NHS Foundation Trust1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2015年2月最近更新:
适应症

试验速览

阶段
不适用
入组人数
70
试验地点
1
主要终点
Responder Rate

研究概览

简要总结

The Investigators have designed this exploratory study in patients suffering from zygapophysial joint mediated pain to investigate if a correlation exists between inter-individual genetic variability (genotype) with treatment response (phenotype). More specifically, the investigators aim to identify any form of correlation between a specific SNP of the BDNF gene (Val66Met) and the effectiveness and/or duration of radiofrequency facet joint neurotomy. The study population is patients suffering from chronic low back pain who have been scheduled for radiofrequency neurotomy following the diagnosis of facet joint mediated pain (using medial branch block test). The investigators will evaluate if a common variant of BDNF gene (Val66Met) can be directly correlated to a significant degree of pain relief following RF treatment, and whether the result of such a procedure can be predicted from a specific genetic profile.

详细描述

Study Hypothesis It is possible to predict individual responsiveness to radiofrequency denervation for zygapophysial (facet) joint mediated pain on the basis of a specific genetic pattern (Single Nucleotide Polymorphism, [SNP])?

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

  • Diagnosed with chronic low back pain which is unresponsive to conservative treatment (including suitable analgesics and physical therapy);
  • Willing to provide consent
  • Subject is capable of comprehending the patient information sheet and has the capacity to give their informed consent to all study procedures in English
  • Be 18 years or older at the time of enrolment;
  • Have specific low back pain that is aggravated by hyperextension and rotation of the spine, with or without hip, buttock or leg pain that does not follow a known dermatomal distribution
  • Paraspinal Tenderness
  • A "positive" response to a uni/bi-lateral MBB* (a response is considered positive when a subject experiences at least 50% reduction in pain scores after the block, regardless of the duration of pain relief)

排除标准

  • Patients who had had any previous back surgery
  • Patients who had previous RF treatments for facet joints mediated pain
  • Patients with another significant cause of low back pain (like spinal stenosis, disc herniation, spondylolisthesis, malignancy, infection or trauma);
  • Radicular pain (pain with neuropathic characteristics following one or more nerve root distribution)
  • Patients with bleeding complications or coagulopathy issues;
  • Concurrent participation in other experimental trials;
  • Known history of adverse reactions to local anesthetics;
  • Pregnant or lactating women;
  • Refusal to provide informed consent for blood banking
  • Any other complication which in the view of the investigator may interfere with the study procedures or the measurement of the accurate study outcomes

结局指标

主要结局

Responder Rate

时间窗: 3 months

Number of patients in each group who report 50% reduction in pain on the visual analogue scale 3 months after radiofrequency denervation for lumbar zygapophysial (facet) joint mediated pain

次要结局

  • Medication intake, Functional status, Ability to work and Quality of life(3 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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