Overview
STACI is a prospective, multicenter, study of SIJ fusion using the iFuse TORQ implant system.
Description
STACI is a prospective, multicenter, study of SIJ fusion using the iFuse TORQ implant system. The goal of the study is to demonstrate the effectiveness of the device for its intended use.
Eligibility
Inclusion Criteria:
- Age > 21 at time of screening
- Patient has lower back / buttock pain for at least 6 months inadequately responsive to non-surgical care
- Diagnosis of sacroiliac joint dysfunction (degenerative sacroiliitis or sacroiliac disruption)
- Baseline Oswestry Disability Index (ODI) score of at least 30%
- Baseline SIJ pain score of at least 5 on 0-10 numerical rating scale
- BMI < 35
- Patient has signed study-specific informed consent form
Exclusion Criteria:
- ASA score 4 or 5
- Severe back pain due to other causes, such as lumbar disc degeneration, lumbar disc herniation, lumbar spondylolisthesis, lumbar spinal stenosis, lumbar facet degeneration, and lumbar vertebral body fracture
- Other known sacroiliac pathology such as: inflammatory sacroiliitis (e.g., ankylosing spondylitis or other HLA-associated spondyloarthropathy), tumor, infection, acute fracture
- Cluneal neuralgia
- Previous SIJ implant placement, including allograft
- Anatomic anomalies/defects that would preclude safe and/or biomechanically acceptable device placement
- History of recent (<1 year) major trauma to pelvis
- Previously diagnosed or suspected severe osteoporosis (defined as prior T-score < -2.5 or history of osteoporotic fracture).
- Chronic rheumatologic condition (e.g., rheumatoid arthritis)
- Current diagnosis of fibromyalgia
- Known allergy to titanium or titanium alloys
- Current local or systemic infection that raises the risk of surgery
- Patient currently receiving or seeking worker's compensation, disability remuneration, and/or involved in injury litigation
- Currently pregnant or planning pregnancy in the next 2 years (self-reported)
- Patient is a prisoner or a ward of the state.
- Known or suspected active drug or alcohol abuse, including opioids
- Diagnosed psychiatric disease (e.g., schizophrenia, major depression, personality disorders) that could interfere with study participation
- Currently participating in another interventional clinical trial
