跳至主要内容
临床试验/NCT05645497
NCT05645497招募中不适用

Evaluation of the Efficacy and Safety of the FACET FIXation Implant Compared With Pedicle Screw Fixation in Patients With Degenerative Lumbar Spinal Stenosis.

SC Medica1 个研究点 分布在 1 个国家目标入组 116 人开始时间: 2023年1月17日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
SC Medica
入组人数
116
试验地点
1
主要终点
The rate of fusion

研究概览

简要总结

This is a single center, hybrid retrospective and prospective (ambispective) study to evaluate the safety and efficacy of the Facet Fixation implant.

The main objective is to evaluate the efficacy of the Facet Fixation implant compared with pedicle screw fixation to determine successful fusion in radiographic assessment at more than two years. Fusion is mainly defined as any sign of bony fusion between the facet joints or transverse processes when viewing the postoperative CT-scan at over 2 years.

详细描述

The primary endpoint is the successful fusion rate in radiographic assessment at more than 2 years.

研究设计

研究类型
Observational
观察模型
Case Control
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 old at the time of the surgery
  • The first back operation in the patient's life was for degenerative lumbar spinal stenosis
  • Surgical treatment of degenerative lumbar spinal stenosis by lumbar decompression with Pedicle Screw fixation or FACET FIXation implant.
  • Patient is able to understand the information related to the study
  • Patient consents to participate to the clinical investigation and agrees (non-objection) on the use of his/her personal data.

排除标准

  • Patient received FACET FIXation implant or Pedicle Screw fixation with supplemental interbody cages.
  • Unilateral Pedicle Screw or FACET FIXation implant.
  • Preoperative grade ≥II spondylolisthesis
  • Preoperative scoliotic deviations >25°.
  • Protected patient (under legal protection, deprived of liberty by judicial or administrative decision).
  • Patient not covered by a social security scheme.

结局指标

主要结局

The rate of fusion

时间窗: 2 years

The proportion of patients achieving the primary endpoint will be evaluated. The rate of fusion in the radiographic assessment is considered successful if all of the following criteria are achieved : * Evidence of bridging bone between the facet joints (Facet Fixation implant) or the transverse processes (pedicle screws) via computed tomography scan. * and ≤ 3mm translational motion between vertebrae on flexion / extension via dynamic X-rays. * and no evidence of lucency surrounding the device (≤25%). The main analysis will compare the successful fusion rate at 2+ years post-operative between the group with the Facet Fixation and the group with pedicle screws, by a confidence interval approach.

次要结局

未报告次要终点

研究者

发起方
SC Medica
申办方类型
Industry
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验