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临床试验/NCT04003714
NCT04003714已完成不适用

EFFECTIVENESS OF REPETITIVE TRANSCRANIAL MAGNETIC STIMULATION IN PATIENTS WITH FAILED BACK SURGERY SYNDROME A DOUBLE-BLINDED, RANDOMISED, PLACEBO CONTROLLED TRIAL

Fatih Sultan Mehmet Training and Research Hospital0 个研究点目标入组 20 人开始时间: 2014年5月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
20
主要终点
Visual Analogue Scale

研究概览

简要总结

Failed back surgery syndrome (FBSS) is the term of persistent back and/or leg pain after surgery for lumbar disk herniation (LDH). Repetitive transcranial magnetic stimulation (r-TMS) is a technique that allows non-invasive and relatively painless stimulation of cerebral cortex. It can reduce the experience of chronic pain by using magnetic field to produce small electrical currents in the cortex.The aim of this study is to determine the effectiveness of r-TMS treatment on patients with FBSS.

详细描述

Methods: In this double-blinded, randomized, placebo-controlled trial, 20 patients (aged 34-65 years) clinically diagnosed as FBSS, who had a history of surgery for LDH with persistent back and leg pain. Patients in r-TMS group received 5 Hz of r-TMS, as a 20-min (1000 pulses) daily session, 5 days per weeks, for a total of 10 sessions. R-TMS applied with MagVenture device (MagPro X100, Denmark, 2009) and figure eight coil (MMC 140 parabolic, MagVenture). Control group received sham r-TMS with the same protocol. Patients were assessed at baseline,after 5th and 10th sessions and 1 and 3 months after treatment. Visual Analogue Scale (VAS), DN-4 (Douleur Neuropathique-4 Questionnaire), Oswestry Disability Index (ODI), Beck Depression Inventory (BDI), Pittsburgh Sleep Quality Index (PSQI) were used for evaluation.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Aged 34-65 years
  • •Clinically diagnosed as FBSS
  • •History of surgery for LDH with persistent back and leg pain
  • •Patients with no root compression in postoperative magnetic resonance imaging of lumbar spine

排除标准

  • •Head trauma
  • •History of intracranial operation
  • •Cardiac pacemaker
  • •Pregnancy
  • •Postoperative lumbar root compression
  • •Neurologic deficits
  • •Prior physiotherapy for low back pain last 6 month

研究组 & 干预措施

Repetitive Transcranial Magnetic Stimulation Group

Experimental

Patients in r-TMS group received r-TMS 20-min (1000 pulses) daily session, 5 days per weeks, for a total of 10 sessions.

干预措施: Repetitive Transcranial Magnetic Stimulation (Device)

Sham Group

Sham Comparator

Control group received sham r-TMS with the same protocol.

干预措施: Sham Repetitive transcranial Magnetic Stimulation (Device)

结局指标

主要结局

Visual Analogue Scale

时间窗: 4 months

All groups were evaluated for low back and leg pain with Visual Analogue Scale (VAS) for rest, activity, and sleep-disturbing. Patients were instructed to indicate the severity of pain on a 10- point scale, on which 0 meant no pain, 5 meant moderate pain, and 10 meant intolerable pain.

DN-4 Interview Questionnaire

时间窗: 4 months

The DN4-interview questionnaire (0-10) was used to identify neuropathic pain.

Oswestry Disability Index

时间窗: 4 months

Functional status in all groups was evaluated with the Oswestry disability index (ODI). The ODI consists of 10 topics concerning pain, lifting, ability of selfcare, ability to walk, sit, stand and travel, social life, and sleep quality and is intended to assess disability and quality of life related to low back pain. ODI scores range from 0 (no disability) to 100 (maximum disability possible).

次要结局

  • The Pittsburgh Sleep Quality Index(4 months)
  • Beck Depression Inventory(4 months)

研究者

发起方
Fatih Sultan Mehmet Training and Research Hospital
申办方类型
Other
责任方
Sponsor

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