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Clinical Trials/NCT02110186
NCT02110186
Unknown
Not Applicable

A Prospective, Comparative Study to Evaluate Effectiveness and Safety of Dynamic Stabilization in Treatment of Lumbar Disc Herniation

Third Military Medical University1 site in 1 country195 target enrollmentJuly 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Lumbar Disc Herniation
Sponsor
Third Military Medical University
Enrollment
195
Locations
1
Primary Endpoint
Range of motion in sagittal plane at the operated level
Last Updated
12 years ago

Overview

Brief Summary

The purpose of this study is to compare safety and outcomes of the following treatments of lumbar disc herniation: (1) discectomy with posterior dynamic stabilization with those of (2) discectomy alone or (3) discectomy with internal fixation and fusion.

Discectomy with posterior dynamic stabilization is proposed as the most effective treatment to improve range of motion, and to be similarly effective to discectomy alone and discectomy with internal fixation and fusion for other functional outcomes after surgery.

Detailed Description

The purpose of this study is to compare outcomes of (1) discectomy with posterior dynamic stabilization with those of (2) discectomy alone or (3) discectomy with internal fixation and fusion. Study aims are: 1. To demonstrate superiority of discectomy with posterior dynamic stabilization over discectomy alone and discectomy with internal fixation and fusion in range of motion at the operated level; 2. To demonstrate non-inferiority of discectomy with posterior dynamic stabilization compared to discectomy alone and discectomy with internal fixation and fusion in functional outcomes as measured by change in Oswestry Disability Index; 3. To compare radiological, clinical, patient-reported and safety outcomes among the three surgical approaches.

Registry
clinicaltrials.gov
Start Date
July 2012
End Date
June 2019
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Qiang Zhou, MD. PhD.

Deputy Chair of the Department of Orthopedics, Chair of the Department of Spine Surgical Group

Third Military Medical University

Eligibility Criteria

Inclusion Criteria

  • Signed informed consent
  • Age between 20 and 60 years inclusive
  • Radiographic evidence of single level lumbar disc herniation
  • Scheduled for single-level lumbar discectomy with or without fusion or dynamic stabilization
  • Preoperative ODI ≥ 30
  • Clinical symptoms consistent with lumbar disc herniation determined by history or physical exam:
  • Radicular back or lower extremity pain and/or
  • Decreased muscular strength and/or
  • Abnormal sensation
  • Involved disk at the spinal level between L2 and S1

Exclusion Criteria

  • Cauda equine syndrome
  • Previous spinal surgery, except previous discectomy at the same segment
  • Patients with other lumbar conditions that will, in the opinion of the investigator, interfere with clinical outcomes (e.g. spinal structural deformities, spinal fractures, ankylosing spondylitis, spinal tuberculosis, spinal infection, spinal tumors, symptomatic cervical spinal disease)
  • Osteoporosis defined as T-score ≤ -2.
  • BMD will be measured by DEXA performed on lumbar spine
  • Systemic infection such as AIDS, HIV, and active hepatitis
  • Recent history (less than 3 years) of chemical substance dependency or significant psychosocial disturbance, which may impact the outcome or study participation
  • Participation in a clinical trial of another investigational drug or device within the past 30 days

Outcomes

Primary Outcomes

Range of motion in sagittal plane at the operated level

Time Frame: 24 months

Mean Change in Oswestry Disability Index (ODI)

Time Frame: Baseline, 24 months

Secondary Outcomes

  • Change in Lumbar Pain Numeric Rating Scale (NRS)(Baseline, 24 months)
  • Change in Leg Pain NRS(Baseline, 24 months)

Study Sites (1)

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