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A Pilot Study of the InterCushion Disc Nucleus Prosthesis (DNP) in Patients Receiving Discectomy

2016年11月1日 更新者:Vertebral Technologies, Inc.

A Pilot Clinical Study to Assess the Safety and Effectiveness of the InterCushion Disc Nucleus Prosthesis in Patients Receiving Discectomy

The primary endpoints of the investigation will include assessment of the maintenance of disc height demonstrated by radiographic evidence based on plain radiographs and MRI and relief of pain as measured by Visual Analog Scale (VAS) at six months post-surgery. It is anticipated that outcomes with the InterCushion Disc Nucleus Prosthesis (DNP) will be comparable to or better than the historical published results for discectomy alone.

研究概览

详细说明

All patients will be followed for at least 24 months once enrolled in the study. Clinical evaluations will be conducted before surgery (baseline), intraoperative, 2 week (± 1 week), 6 week (± 1 week), 3 months (± 2 weeks), 6 months (± 1 month), 12 months (± 2 months) and 24 months (± 2 months).

研究类型

观察性的

注册 (预期的)

100

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Manitoba
      • Brandon、Manitoba、加拿大、R7A 2B3
        • 招聘中
        • Brandon Regional Health Center
        • 接触:
        • 接触:
        • 首席研究员:
          • Phillip de Mueleneare, MD

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

21年 至 60年 (成人)

接受健康志愿者

不

有资格学习的性别

全部

取样方法

非概率样本

研究人群

The protocol includes skeletally mature patients, both male and female, 18 to 60 years old suffering from a herniated disc (confirmed by X-ray, CT or MRI) with persistent leg pain.

描述

Inclusion Criteria:

  • Patient has signed and dated a study specific informed consent form approved by the reviewing Institutional Review Board or Ethics Committee.
  • Patient is 21 to 60 years of age.
  • Patient is skeletally mature
  • Patient requires a discectomy of one level from L2-S1.
  • Patient has less than 50% loss of disc height at the affected level.
  • Patient has persistent pain (predominantly leg pain, although some back pain that occurred at the same time as the leg pain and is believed to be associated with the disc herniation will not disqualify the patient from participating in this study) and symptoms despite a minimum of six weeks of non-operative treatment.
  • Patient X-ray, CT or MR evidence of a herniated disc at the affected level.
  • Patient has a minimum leg pain score of 6 cm on a 10 cm (i.e. 60 mm on a 100 mm) point visual analog scale (VAS).
  • Patient has a minimum Oswestry Disability Index score of 40% (based upon a 100% scale).
  • Patient is physically and mentally willing and able to comply with the postoperative scheduled clinical and radiographic evaluations and rehabilitation.

Exclusion Criteria:

  • Patient has had any previous surgery at the affected levels.
  • Patient has had any attempt at spinal fusion, at any lumbar levels.
  • Patient has motion of < 3 degrees on pre-operative lateral flexion/extension radiographs
  • Patient has a BMI
  • Patient has severe osteoporosis of the spine.
  • Patient has previously undergone chemotherapy, immunosuppressive therapy or radiation to the local area.
  • Patient has active local or systemic infection.
  • Patient has any known active malignancy.
  • Patient has rheumatoid arthritis or systemic lupus erythematosus, or other chronic, inflammatory autoimmune disorder.
  • Patient has ankylosing spondylitis or other spondyloarthropathy.
  • Patient has spondylolisthesis.
  • Patient is pregnant or plans to become pregnant during the course of the study.
  • Patient has other concurrent physical or mental conditions that are likely to affect their outcome.
  • Patient has congenital stenosis
  • Patient is diabetic.
  • The patient has osteoporosis or severe osteopenia as determined by the Investigator. Females over 40 with bone density score less than -1. A clinical SCORE calculator may also be utilized for females over 40 years of age.
  • Patient has significant facet disease.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

队列和干预

团体/队列
干预/治疗
Disc Nucleus Replacement
Disc Nucleus Replacement (InterCushion DNP)
The device is intended for spinal arthroplasty in skeletally mature patients with leg pain due to a herniated disc with or without back pain, who are having a discectomy at one level from L2 -S1. These patients should have no spondylolisthesis at the involved level.
其他名称:
  • InterCushion Disc Nucleus Prosthesis (DNP)

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Decrease in ODI
大体时间:6 months
Improvement in the Oswestry Disability Index (ODI) score i.e. decrease of 15% or better ODI.
6 months
Decrease in VAS
大体时间:6 months
Improvement in leg pain evidenced by decrease in pain score of at least 2 cm (i.e. 20 mm) on the visual analog scale (VAS)
6 months
Maintenance of post-operative disc height
大体时间:6 months
Disc at the treated level is collapsed by ≤ 15% when compared to an adjacent health level.
6 months
Mobility of treated segment
大体时间:6 months
Motion of ≥ 3 degrees on lateral flexion/extension radiographs
6 months
Neurologic deficits
大体时间:6 months
No new permanent neurological deficit or worsening of an existing permanent neurological deficit
6 months

次要结果测量

结果测量
措施说明
大体时间
Maintenance or decrease in ODI
大体时间:12 and 24 months
Maintenance of improvement or further improvement in the Oswestry Disability Index (ODI) score measured at six months i.e. decrease of 15% or better ODI.
12 and 24 months
Maintenance or decrease in VAS
大体时间:12 and 24 months
Maintenance of improvement or further improvement in leg pain evidenced by decrease in pain score on the visual analog scale (VAS)
12 and 24 months
Maintenance of post-operative disc height.
大体时间:12 and 24 months
Disc at the treated level is collapsed by ≤ 15% when compared to an adjacent health level.
12 and 24 months
Mobility of treated segment
大体时间:12 and 24 months
Motion of ≥ 3 degrees on lateral flexion/extension radiographs
12 and 24 months
Neurological deficits
大体时间:12 and 24 months
No new permanent neurological deficit or worsening of an existing permanent neurological deficit
12 and 24 months

其他结果措施

结果测量
措施说明
大体时间
Failures
大体时间:6, 12 and 24 months

Revision: is a procedure that adjusts or in any way modifies or removes part of the original implant configuration, with or without replacement of a component.

Removal: is a procedure where the entire original system configuration is removed with or without replacement.

Supplemental fixation: a procedure in which additional instrumentation not under study is implanted.

6, 12 and 24 months

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Phillip F de Muelanaere, MD、Brandon General Hospital

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2012年1月1日

初级完成 (预期的)

2018年1月1日

研究完成 (预期的)

2018年6月1日

研究注册日期

首次提交

2012年7月24日

首先提交符合 QC 标准的

2012年7月26日

首次发布 (估计)

2012年7月27日

研究记录更新

最后更新发布 (估计)

2016年11月2日

上次提交的符合 QC 标准的更新

2016年11月1日

最后验证

2016年11月1日

更多信息

与本研究相关的术语

关键字

其他研究编号

  • CP 2010-001

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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