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临床试验/NCT07627490
NCT07627490尚未招募不适用

The Value of Transcutaneous Electrical Nerve Stimulation (TENS) for Improving Pain Experienced During Posterior Branch Blocks in Patients With Lumbar Posterior Joint Syndrome: a Single-center, Randomized, Double-blind, Parallel-group, Controlled, Superiority Trial

University Hospital, Toulouse1 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2026年9月1日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
52
试验地点
1

研究概览

简要总结

Procedural pain is inadequately managed in two-thirds of patients undergoing invasive medical procedures. Several techniques exist for managing procedural pain, but they all present implementation challenges and are not without side effects. Therefore, a new, non-pharmacological, inexpensive, and easy-to-use approach would be of significant benefit. Transcutaneous electrical nerve stimulation (TENS) for pain relief could represent this alternative. Few studies have been conducted on the benefits of TENS in managing procedural pain, for example, in shoulder arthrodistension. This project proposes to study it in the context of posterior ramus infiltration in patients eligible for this indication, in the context of chronic low back pain associated with posterior joint syndrome.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Participant)

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

  • Chronic low back pain (lasting more than 3 months)
  • Patient followed in a Chronic Pain Unit (CETD, Toulouse University Hospital)
  • Clinical and radiological diagnosis (CT scan or MRI) of posterior joint syndrome
  • Patient with an indication for infiltration therapy, feasible under standard conditions

排除标准

  • Spinal surgery
  • Contraindications for TENS:
  • Wearing an electronic medical device (pacemakers, defibrillators, etc.)
  • Pregnancy
  • Area of cutaneous anesthesia
  • Patient with an active malignant tumor
  • Patient with deep vein thrombosis
  • Patient with damaged or fragile skin
  • Insulin-dependent or uncontrolled diabetes
  • Uncontrolled hypertension
  • Allergy to the local anesthetics used
  • Severe psychiatric disorder
  • Lumbar injection within the previous 6 months

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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