Status:
RECRUITING
Sacroiliac (SI) Joint Transfixing and Fusion: Meaningful Long Term Outcomes With Nevro1
Lead Sponsor:
Nevro Corp
Conditions:
Sacroiliac Joint Dysfunction
Eligibility:
All Genders
21+ years
Brief Summary
The goal of this observational study is to learn if Nevro1 Sacroiliac Transfixing and Fusion System can treat sacroiliac joint dysfunction in males or females over 21. The main questions it aims to an...
Eligibility Criteria
Inclusion
- Has medical insurance that covers this standard of care procedure and all other anticipated and unanticipated procedure-related care, and all coverage criteria required by insurer are met, which may include but are not limited to:
- Has had low back and/or buttock pain for at least 6 months that is inadequately responsive to non-surgical care
- Has a positive Fortin's test
- Has a diagnosis of SIJ dysfunction (degenerative sacroiliitis or SI disruption) with pain elicited on at least 3 of 5 provocative tests (FABER, Gaenslen, Distraction, Thigh Thrust, Compression).
- At least 75% reduction in pain for the expected duration of two anesthetics (on separate visits each with a different duration of action), and the ability to perform previously painful maneuvers, following an image-guided, contrast-enhanced intra-articular (diagnostic) SIJ injection
- A trial of at least one therapeutic intra-articular SIJ injection (i.e. corticosteroid injection)
- Has an ODI score ≥30% at enrollment
- Has a SI joint pain score of at least 5 out of 10 on numerical rating scale at enrollment.
- Be at least 21 years of age at enrollment
- The patient's physician has decided that the best treatment for the patient's SIJ dysfunction is the Nevro1 SI Fixation System, and the patient has agreed to the treatment
- Be willing and capable of giving written informed consent
- Be mentally and physically able to comply with study-related requirements and procedures and attend all scheduled visits
Exclusion
- Has current severe back pain due to other causes, such as lumbar disc degeneration, lumbar disc herniation, lumbar spondylolisthesis, lumbar spinal stenosis, lumbar facet degeneration, lumbar radicular pain, and lumbar vertebral body fracture
- Has SIJ pain secondary to inflammatory conditions or other known sacroiliac pathology such as: Sacral dysplasia, inflammatory sacroiliitis (e.g., ankylosing spondylitis or other HLA-associated spondylo-arthropathy), tumor, infection, acute fracture, and crystal arthropathy
- Has had a previous SIJ implant placement, including an allograft
- Has had an injection with corticosteroid into the index SIJ within the last 30 days
- Has had a sacral radiofrequency ablation within the last 6 months
- Has a history of recent (\<1 year) major trauma to pelvis
- Has previously diagnosed or suspected severe osteoporosis (defined as prior T-score \< -2.5 or history of osteoporotic fracture)
- Has a chronic rheumatologic condition (e.g., rheumatoid arthritis)
- Has a known allergy to titanium or titanium alloys
- Has a current local or systemic infection that raises the risk of surgery
- Is currently receiving or seeking short- or long-term worker's compensation related to the SI joint or low back pain, is currently receiving disability remuneration related to SI joint or low back pain, and/or is currently involved in injury litigation related to the SI joint or low back pain
- Is participating in an investigational study or has been involved in an investigational study within 3 months prior to enrollment
- Has any condition or anatomy that makes treatment with the Nevro1 SI Fixation System infeasible
- Is taking a medication known to have detrimental effects on bone quality and soft tissue healing
- Has a prominent neurologic condition that would interfere with physical therapy
- Be pregnant or plan on becoming pregnant in the next two years.
- Has a medical condition or pain in other area(s), not intended to be treated in this study, that could interfere with study procedures, accurate pain reporting, and/or confound evaluation of study endpoints, as determined by the Investigator
Key Trial Info
Start Date :
April 3 2025
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
June 1 2027
Estimated Enrollment :
180 Patients enrolled
Trial Details
Trial ID
NCT06909292
Start Date
April 3 2025
End Date
June 1 2027
Last Update
April 4 2025
Active Locations (5)
Enter a location and click search to find clinical trials sorted by distance.
1
AIRS Clinic
Lodi, California, United States, 95240
2
Michigan Orthopaedic Surgeons
Southfield, Michigan, United States, 48033
3
Carolinas Pain Institute
Winston-Salem, North Carolina, United States, 27103
4
Advanced Spine and Pain Specialists
Spring, Texas, United States, 77380