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临床试验/NCT04254250
NCT04254250进行中(未招募)不适用

Observational Cohort Study Of The Efficacy Of Preoperative Estimation Of Disc Herniation Recurrence In Patients With Lumbar Disc Herniation

Novosibirsk Research Institute of Traumatology and Orthopaedics n.a. Ya.L. Tsivyan2 个研究点 分布在 1 个国家目标入组 386 人开始时间: 2020年2月10日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
386
试验地点
2
主要终点
Reherniation rate

研究概览

简要总结

This study will be conducted at Research Institute of Traumatology and Orthopedics (NRITO) n.a. Ya.L.Tsivyan, Novosibirsk, Russia.

The current study is prospective observational study to evaluate the efficacy of preoperative estimation of disc herniation recurrence among patients with lumbar disc herniation using predictive mathematical model at terms 3 years postoperatively .

It is expected to enroll 350 patients aged 18-70 with lumbar disc herniation. Risk estimation of disc herniation recurrence will be evaluated preoperatively, then patient will undergo conventional microdiscectomy. Postoperative eximanation will include Visits every 6-months during 3 years to evaluate clinical outcomes.

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 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18 to 60 years;
  • Single level lumbar disc herniation with neural compression confirmed on MRI at one level of L4-L5 or L5-S1;
  • Radicular leg pain with or without back pain;
  • Symptoms persisting for at least four weeks prior to surgery;
  • Given written Informed Consent;
  • Able and agree to fully comply with the clinical protocol and willing to adhere to follow-up schedule and requirements;
  • Visual Analogue Scale score at least 40/100 at baseline.

排除标准

  • More than one symptomatic level requiring multilevel surgical decompression
  • Stenosis any etiology at the same level;
  • Spondylolisthesis any etiology at the same level;
  • Prior lumbar spinal surgery at any level;
  • Other non-degenerative spinal conditions (e.g. infectious, traumatic, metabolic, inflammatory, neoplastic, structural or other pathology) that may have an impact on subject safety, wellbeing or the intent and conduct of the study
  • Concurrent participation in another clinical study that may confound study results.

结局指标

主要结局

Reherniation rate

时间窗: at 3 years follow-up term postoperatively

Rate of lumbar disc reherniation, symptomatic presence of disc herniation confirmed by MRI at the previously operated level and side

次要结局

  • Improvement of Oswestry Disability Index (ODI)(6, 12, 18, 24, 30, 36 months follow up)
  • Change from baseline in EQ-5D (EuroQl - 5 dimensional)(6, 12, 18, 24, 30, 36 months follow up)
  • Improvement of Visual analog scale (VAS) leg pain intensity(6, 12, 18, 24, 30, 36 months follow up)
  • HTI Item (from SF-36)(6, 12, 18, 24, 30, 36 months follow up)

研究者

发起方
Novosibirsk Research Institute of Traumatology and Orthopaedics n.a. Ya.L. Tsivyan
申办方类型
Other Gov
责任方
Sponsor

研究点 (2)

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