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临床试验/NCT02617563
NCT02617563已完成不适用

A Prospective, 5-Year Global Study on MAST™ Minimally Invasive Fusion Procedures for the Treatment of the Degenerative Lumbar Spine

Medtronic Spinal and Biologics26 个研究点 分布在 17 个国家目标入组 361 人开始时间: 2015年12月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
361
试验地点
26
主要终点
Improvement of disability, Oswestry Disability Index (ODI) as compared to baseline in DDD patients with spondylolisthesis

研究概览

简要总结

The purpose of this study is

  • to evaluate the effectiveness of MAST techniques for anterior/lateral and posterior approaches in Degenerative Disc Disease (DDD) patients with spondylolisthesis (≥ grade I).
  • To assess how single or double level MAST(Minimal Access Spinal Technologies) fusion procedures PLIF (Posterior Lumbar Interbody Fusion), TLIF (Transforaminal Lumbar Interbody Fusion), DLIF (Direct Lateral Interbody Fusion), OLIF (Oblique Lumbar Interbody Fusion), ALIF (Anterior Lumbar Interbody Fusion), or MIDLF (Midline Lumbar Interbody Fusion) are used in surgical practice and to describe long-term safety and effectiveness in a broad patient population of patients with degenerative lumbar disc disease .

详细描述

In this Prospective, Global (multi center), Post Market Release (PMR) Study, Patients will be submitted to a single or double level instrumented fusion procedure using a PLIF, TLIF, ALIF, OLIF, DLIF or MIDLF technique via a minimally invasive procedure and will receive the same medical treatment as if they would not participate in this study.

  • The study will be monitored with visits conducted at the start, during and at the closure of the clinical study.
  • MedDRA coding will be used to classify the Adverse Event.
  • The study will be conducted according to Medtronic SOPs
  • Sample size calculation: Assuming that the standard deviation for ODI improvement at 3 months is 20 for both groups (anterolateral and posterior) and there is no difference in the mean ODI improvement at 3 months, with 80% power and 5% alpha level, the sample size for the primary endpoint (DDD patients operated for spondylolisthesis) is as follows in order to claim equivalence between two groups with equivalent margin (-10, 10):
  • Estimated sample size per group (anterolateral procedures versus posterior procedures): 70
  • Estimated total sample size for spondylolisthesis patients: 140
  • From the MASTERS-D study it is know that approximately 50% of the patients with degenerative disc disease have spondylolisthesis ≥ grade I. Hence the required total sample size is 140/0.5 = 280. The study is anticipated to enroll 350 patients.
  • In addition to a final statistical analysis, 3 months and annual interim analyses are anticipated.
  • The study hypothesis for the primary objective is to verify whether patients operated for spondylolisthesis (≥ grade I) have equivalent mean improvement of ODI at 3 months regardless of the minimally invasive surgical procedure (anterolateral or posterior) used.
  • The null-hypothesis: Ho: Δ ODI_Anterolateral ≠ Δ ODI_posterior
  • will be tested against the alternative hypothesis: HA: Δ ODI_Anterolateral = Δ ODI_posterior Where Δ ODI_Anterolateral is the average improvement in ODI score (baseline - 3 months) in spondylolisthesis subjects treated with the anterolateral approach and Δ ODI_posterior is the average improvement in ODI score (baseline - 3 months) in spondylolisthesis subjects treated with the posterior approach.

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

  • Patient is ≥ 18 years of age (or minimum age as required by local regulations)
  • Patient has degenerative disc disease and an indication for a single or double level instrumented lumbar fusion for the treatment
  • Patient agrees to participate in the study and is able to sign the Data Release Form/Informed Consent
  • The procedure planned for the patient complies with the labeling of the Devices that may be used in the surgical procedure as described in the section Medical Devices of the Clinical Investigation Plan
  • Patient is planned to be submitted to a minimally invasive fusion procedure using a posterior (PLIF, TLIF, MIDLF) or anterolateral (OLIF, ALIF, DLIF ) technique*
  • *For a double level instrumented fusion, the same procedure must be used for both levels.
  • The patient is willing and is able to perform study procedures and required follow-up visits.

排除标准

  • Patient that has already undergone a lumbar fusion surgery
  • Patient that has already undergone open lumbar surgery other than standard decompression surgery
  • Indications for the procedure other than degenerative spine disease like: Osteoporotic vertebral fractures, Spine trauma fractures or Spine tumor
  • Illiterate or vulnerable patients (e.g. minors, participants incapable of judgment or participants under tutelage)
  • Concurrent participation in another clinical study that may confound study results.

结局指标

主要结局

Improvement of disability, Oswestry Disability Index (ODI) as compared to baseline in DDD patients with spondylolisthesis

时间窗: 3 months

To demonstrate that DDD patients operated for spondylolisthesis fare equally well regardless of the surgical procedure (anterolateral or posterior) performed as measured by the improvement of ODI at 3 months as compared to baseline.

次要结局

  • Improvement of Visual analog scale (VAS) back pain intensity(Through 5 years)
  • Improvement of VAS leg pain intensity(Through 5 years)
  • Improvement of EQ-5D(Through 5 years)
  • The neurological success rate defined as maintenance or improvement of neurological functions(Through 5 years)
  • Amount of days needed for first ambulation(From surgery up to hospital discharge)
  • Improvement of ODI(Through 5 years)
  • Health economics evaluation(Through 5 years)
  • Fusion success(Through 5 years)
  • Amount of days needed to recover from Surgery(Surgery Recovery Day up to hospital discharge)
  • Improvement of disability ODI as compared to baseline in DDD patients without spondylolisthesis(3 months)
  • Proportion of patients needing a second surgery at the index and/or adjacent level(s) (reoperation rates) throughout the study(Through 5 years)
  • Adverse Events(Through 5 years)
  • Comparison of Patient profile at baseline with minimally invasive fusion procedure performed(Baseline to surgery)

研究者

发起方
Medtronic Spinal and Biologics
申办方类型
Industry
责任方
Sponsor

研究点 (26)

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