跳至主要内容
临床试验/NCT04461964
NCT04461964撤回不适用

Single Center, Prospective Study of the MvIGS Spine Navigation System in Posterior Fusion Utilizing Pedicle Screw Fixation

NYU Langone Health0 个研究点开始时间: 2022年7月最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
主要终点
Total length of operative time

研究概览

简要总结

The goal of this study is to prospectively collect information about the operative time and intraoperative radiation experienced by patients undergoing posterior spinal fusion procedures guided by the MvIGS spine navigation system.

详细描述

This is a single-center, prospective case series to assess the use of the Machine-vision Image Guided Surgery (MvIGS) spine navigation system for treatment of spinal stenosis, scoliosis, and spondylolisthesis that requires fusion. This is a single-arm, open-label study. All participants will undergo their single and multi-level posterior spine fusion surgery using bilateral pedicle screw instrumentation under MvIGS intraoperative navigation guidance.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosis of spinal stenosis of the lumbar spine with degenerative spondylolisthesis, all grades, and planning to undergo surgical fusion;
  • Skeletally mature adults between the ages of 18-85 years at the time of surgery;
  • Has completed at least 6 months of conservative therapy for degenerative diagnosis, if appropriate; and,
  • Personally signed and dated an informed consent document prior to any study-related procedures, indicating that the patient has been informed of all pertinent aspects of the study.

排除标准

  • History of malignancy, craniocervical junction pathology, cervical and thoracic locations, and/or previous lumbar operation;
  • Significant peripheral neuropathy or acute denervation secondary to radiculopathy, caused by conditions other than spinal stenosis;
  • Significant peripheral vascular disease (defined as diminished dorsalis pedis or tibial pulses);
  • Morbid obesity, defined as BMI > 40 kg/m2;
  • Active systemic or local infection;
  • Active hepatitis (defined as receiving medical treatment within two years);
  • Immunocompromised, such as but not limited to being diagnosed with Acquired Immunodeficiency Syndrome (AIDS), HIV infection, Severe Combined Immunodeficiency Syndrome, or Thymic Hypoplasia;
  • Insulin-dependent diabetes mellitus or any other medical condition(s) that would represent a significant increase in surgical risk or interfere with normal healing;
  • Immunologically suppressed, or has received systemic steroids, excluding nasal steroids, at any dose daily for > 1 month within last 12 months;
  • History of Paget's disease, osteomalacia, or any other metabolic bone disease;
  • Involved in study of another investigational product that may affect outcome;
  • Women who are pregnant, lactating or anticipate becoming pregnant within 24 months post-surgery;
  • Non-English speaking;
  • Patients who are incarcerated;
  • Worker's compensation cases; or,
  • Patients involved in active litigation relating to his/her spinal condition.

结局指标

主要结局

Total length of operative time

时间窗: Visit 1 Day 1

The aim is to reduce operative time. Operative time will be determined by the official recorded operative notes.

次要结局

  • Length of time to register images(Visit 1 Day 1)
  • Time to ambulation(Post operative hospital visit (Day 1-10))
  • Time to hospital discharge after surgery(Post operative hospital visit (Day 1-10))
  • Screw placement accuracy(Visit 1 Day 1)
  • Length of time to place all screws(Visit 1 Day 1)
  • Estimated blood loss (EBL)(Visit 1 Day 1)
  • Dose of intraoperative ionizing radiation(Visit 1 Day 1)
  • incidence of intraoperative complications(Visit 1 Day 1)

研究者

申办方类型
Other
责任方
Sponsor

相似试验

Effects of a Spine Navigation System on Op-time and... | 临床试验