跳至主要内容
临床试验/NCT00760799
NCT00760799已完成4 期

Randomized Study of Anular Repair With the Xclose Tissue Repair System

Anulex Technologies, Inc.34 个研究点 分布在 1 个国家目标入组 750 人开始时间: 2007年3月1日最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
已完成
入组人数
750
试验地点
34
主要终点
Re-operations due to re-herniation (repeat discectomy procedure)

研究概览

简要总结

The purpose of this study is to evaluate the benefits of anulus fibrosus repair utilizing Xclose™ compared to a discectomy without anulus fibrosus repair.

详细描述

Discectomy surgery is intended to remove the impinging fragment on the nerve root thus alleviating the pain and providing the nerve with a better healing environment. Discectomy procedures entail removing a bony portion of the vertebral body to access the posterior side of the disc space, and then removing the impinging fragment from the disc. The fragment being removed can either be contained within the wall of the anulus, which requires incision into the anulus to remove it, or it could be extruded through an anular fissure. In the absence of a safe and easy method to close or seal the defect in the anulus following a discectomy procedure, surgeons are left with no alternative but to leave the anulus in this compromised state which is largely the current practice. This rent in the soft tissue of the anulus fibrosus can lead to postoperative problems if the remaining nuclear tissue in the disc pushes through the anular defect or incision causing recurrent or persistent pain.

Initial studies involved the placement of sutures to seal the anular defect. This work strongly suggested that microsurgical anular reconstruction can reduce recurrent herniations and re-operations, post discectomy. Unfortunately, this technique is not easy to perform and may pose an increased risk to the patient.

This study utilizes the Xclose™ Tissue Repair System to re-approximate the compromised tissue of the anulus fibrosus in appropriately randomized patients in an effort to quantify the benefits of anular repair for discectomy patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

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

入选标准

  • •Candidate for a one or two level discectomy
  • •Positive imaging evidence of intervertebral disc herniation at location corresponding to patient's radicular signs or symptoms
  • •Anular tear or slit incision and additionally deemed to include sufficient tissue for tissue reapproximation
  • •Persistent and predominant radicular pain
  • •Pre-operative leg pain score > 4.0 cm on a 10 cm Visual Analog Scale (VAS)
  • •Leg pain unresponsive to conservative treatment (physical therapy and non-steroidal anti-inflammatory medical therapy) for 6 or more weeks; exception, individuals suffering from acute and uncontrollable severe leg pain
  • •Patient is willing and able to comply with study requirements; willing and able to sign a study-specific, informed consent form, complete necessary study paperwork and return for required follow-up visits.

排除标准

  • •Age less than 18 years
  • •Prior or planned surgical procedure intended to fuse or stabilize the lumbar spine
  • •Previous surgery involving index level
  • •Cauda Equina Syndrome
  • •Evidence of severe disc degeneration
  • •Greater than Grade I spondylolisthesis or retrolisthesis at the affected level
  • •No apparent anular defect and no indication to open the anulus at time of procedure
  • •Active local or systemic infection
  • •Active malignancy or other significant medical co-morbidities
  • •Current chemical dependency or significant emotional and/or psychosocial disturbance that would impact treatment outcome or study participation
  • •Patient or legal guardians who are unwilling or unable to cooperate or give written informed consent
  • •Women who are pregnant or with child bearing potential and who are not on a reliable form of birth control
  • •Current fracture, tumor and/or deformity (> 15° of lumbar scoliosis, using Cobb measuring technique) of the spine
  • •Documented history of allergy or intolerance to PET
  • •Patient is currently enrolled in other research that could confound the results of the study.

研究组 & 干预措施

1

Active Comparator

Standard discectomy without anular repair

干预措施: Discectomy with anular repair (Procedure)

2

Experimental

Standard Discectomy with anular repair

干预措施: Discectomy with anular repair (Procedure)

结局指标

主要结局

Re-operations due to re-herniation (repeat discectomy procedure)

时间窗: 2 wks and at 6, 12, 18 and 24 months

次要结局

  • Patient outcomes (utilizing Oswestry Disability Index, Visual Analog Scale and SF-12 quality of life assessment), Health care utilization, Return to work(2 weeks and at 6, 12, 18, and 24 months)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (34)

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