Phase
Condition
Chronic Pain
Spinal Stenosis
Spondylolisthesis
Treatment
N/AClinical Study ID
Ages > 18 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Subjects enrolled in this study must meet ALL of the following inclusion criteria:
- Subject must provide written informed consent prior to any clinical study-relatedprocedure.
- Subject is at least 18 years or older at the time of enrollment, skeletal mature.
- Subject has 1-2 symptomatic lumbar degenerative disease at adjacent level,T12-S1, with or without grade I spondylolisthesis (confirmed by history andradiographic studies).
- MRI within 12 months prior to the procedure with at least mild to moderate spinalstenosis at the index treatment level
- Subject has undergone at least 3 months of non-operative treatment.
- Subject presents with ZCQ physical function ≥ 2.0 at baseline.
- Subject reports relief from lumbar flexion and/or sitting.
- Subject has baseline VAS of back and/or leg pain standing or walking ≥ 50mm.
Exclusion
Exclusion Criteria:
- Subjects enrolled in this study must NOT meet any of the following exclusion criteria:
- Subject is unable to provide written informed consent.
- Subject has had previous lumbar spine surgery at the intended treatment level (e.g., laminectomy or fusion).
- Subject has a grade II or greater spondylolisthesis on flexion and extensionradiographs with 3mm instability.
- Subject has confirmed or suspected osteoporosis or osteopenia.
- Subject is enrolled, or intends to participate, in a clinical drug and/or devicestudy (investigational device, investigational drug, new indication for a deviceor drug, or additional testing beyond standard of care procedures) which couldconfound the results of this trial as determined by the investigator.
- Presence of other anatomic or comorbid conditions, or other medical, social, orpsychological conditions that, in the investigator's opinion, could limit thesubject's ability to participate in the clinical investigation or to comply withfollow-up requirements.
- Subject is pregnant or nursing.
Study Design
Study Description
Connect with a study center
Evolve Restorative Center
Santa Rosa, California 95403
United StatesSite Not Available
The Raso Pain Center
Jupiter, Florida 33477
United StatesActive - Recruiting
Koga Neurosurgery
Slidell, Louisiana 70458
United StatesActive - Recruiting
National Spine and Pain Centers
Oxon Hill, Maryland 20745
United StatesActive - Recruiting
Comprehensive & Interventional Pain Management
Henderson, Nevada 89509
United StatesActive - Recruiting
Nevada Advanced Pain Specialists
Reno, Nevada 20745
United StatesActive - Recruiting
Reno Tahoe Pain Associates
Reno, Nevada 89509
United StatesActive - Recruiting
The Pain Management Center
Voorhees, New Jersey 08043
United StatesActive - Recruiting
Premier Pain Treatment Institute
Loveland, Ohio 45140
United StatesActive - Recruiting
Center for Interventional Pain and Spine
Chadds Ford, Pennsylvania 17601
United StatesActive - Recruiting
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