N/A
N=168
The STEPS - Totalis™ Trial
Lumbar Spinal Stenosis
Bottom Line
View on ClinicalTrials.gov: NCT02079038 ↗Enrolled (actual)
168
Serious AEs
17.9%
Results posted
Aug 2020
Primary outcome: Primary: Percentage of Subjects With Clinically Significant Improvement in Outcomes — 56.3; 56.0 percentage of subjects
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Totalis (Device); Comparator Surgical Procedure (Procedure)
- Age
- Adult, Older Adult · 55+ yrs
- Sex
- All
- Sponsor
- VertiFlex, Incorporated
- Primary completion
- Jan 2017
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Percentage of Subjects With Clinically Significant Improvement in Outcomes |
56.3; 56.0 | — |
Summary
The purpose of this study is to determine safety and effectiveness, as measured by changes in pain, disability, patient satisfaction, and claudicatory symptoms, at 6 months following treatment with the Totalis™ Direct Decompression System or Sham Comparator Surgical Procedure in patients with lumbar spinal stenosis
Eligibility Criteria
Inclusion Criteria
- Male or female subjects greater than or equal to 55 years of age
- Neurogenic intermittent claudication (NIC) symptoms defined generally as leg/buttock/ groin pain and/or paresthesias that are exacerbated with standing and walking and relieved by flexion
- VAS leg symptom severity >50 (in either leg) during episodes of neurogenic claudication
- Subjects who are able to walk a minimum of 50 feet without experiencing NIC symptoms
- Diagnosis of central canal spinal stenosis, with or without mild to moderate lateral recess stenosis, at one or two levels from L1-L5 with radiologic evidence
- Subjects with persistent lumbar spinal stenosis symptoms that, during the course of the last year, have been unresponsive to a minimum of 6 months of conservative therapy
Exclusion Criteria
- Significant back, buttock or leg pain from causes other than lumbar central canal stenosis
- Axial back pain only
- Severe foraminal stenosis at index level(s) and/or symptomatic foraminal stenosis at any lumbar level
- Severe lateral recess stenosis
- Lumbar spinal stenosis at more than two levels determined pre-operatively to require surgical intervention
- Prior decompressive surgery at index level (s) or fusion at any lumbar level
- Epidural steroid or nerve block steroid injection at index level(s) within 6 weeks of baseline assessments
- Spondylolisthesis (anterolisthesis or retrolisthesis) greater than grade 1
- Spondylolysis (pars fracture)
- Significant degenerative lumbar scoliosis at index level(s)
- Morbid obesity
- Significant peripheral vascular disease
- Active significant co-morbidity
- Undergoing immunosuppressive therapy or long-term steroid use
- Current spinal cord stimulator or implanted pain pump
- Life expectancy less than 2 years
- Evidence of substance abuse within the year
- Involvement or potential involvement in litigation related to the spine or worker's compensation related to a back and/or leg issue
Data sourced from ClinicalTrials.gov (NCT02079038). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.