iFuse Implant System® Minimally Invasive Arthrodesis
CompletedNot applicableNCT01741025
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This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
The purpose of this study is to compare outcomes when patients with chronic sacroiliac joint pain undergo either SI joint fusion with the iFuse Implant System or undergo conservative management of the SI joint
Study details
- Official title
- A Multicenter Randomized Controlled Post-market Clinical Follow-up Trial Comparing the Effectiveness and Safety of the iFuse Implant System® Versus Conservative Management for Patients With Chronic, Disabling SI Joint Pain.
- Conditions
- Sacroiliac Joint Pain
- Interventions
- Device: iFuse Implant System
- Other: Conservative Management
- Sponsor
- SI-BONE, Inc.
- Start date
- 2013-06
- Primary completion
- 2015-12-15
- Sex
- All
- Age range
- from 21 Years to 70 Years
- Results posted
- No results posted in this snapshot
- Countries
- Belgium, Germany, Italy, Sweden
- Total sites listed
- 9
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: 1. Age 21-70 at time of screening 2. Patient has lower back pain for \>6 months or \>18 months for pregnancy induced lower back pain 3. Diagnosis of the SI joint as the primary lower back pain generator based on ALL of the following: a. Patient has pain at or close to the posterior superior iliac spine (PSIS) with possible radiation into buttocks, posterior thigh or groin and can point with a single finger to the location of pain (Fortin Finger Test), and b. Patient has at least 3 of 5 physical examination maneuvers specific for SI joint pain, and c. Patient has improvement in lower back pain NRS of at least 50% of the pre injection NRS score after fluoroscopic controlled injection of local anesthetic into affected SI joint(s) (including previous documented test \<6 months ago) 4. Baseline Oswestry Disability Index (ODI) score of at least 30% 5. Baseline lower back pain score of at least 50 on 0-100 point VAS 6. Patient has signed study-specific informed consent form 7. Patient has the necessary mental capacity to participate and is physically able to comply with study protocol requirements Exclusion Criteria: 1. Severe lower 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 2. Sacroiliac pathology caused by auto-immune disease (e.g. ankylosing spondylitis) and/or neoplasia (e.g. benign or malignant tumor) and/or crystal arthropathy 3. History of recent (\<1 year) fracture of the pelvis with documented malunion, non-union of sacrum or ilium or any type of internal fixation of the pelvic ring. 4. Spine surgery during the past 12 months. 5. Previously diagnosed or suspected osteoporosis (defined as prior T-score \<-2.5 or history of osteoporotic fracture) 6. Documented osteomalacia or other metabolic bone disease 7. Any condition or anatomy that makes treatment with the iFuse Implant System infeasible 8. Known allergy to titanium or titanium alloys 9. Use of medications known to have detrimental effects on bone quality and soft-tissue healing 10. Prominent neurologic condition that would interfere with physical therapy 11. Current systemic infection or local infection at the SI joint 12. Currently pregnant or planning pregnancy in the next year 13. Known or suspected drug or alcohol abuse 14. Diagnosed psychiatric disease (e.g., schizophrenia, major depression, personality disorders) that c…
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT01741025