Clinical Research Directory

Inclusion Criteria: * Subject scheduled for open posterior lumbosacral arthrodesis (including at least the following three vertebrae: L4, L5 and S1) associated with a sacroiliac fusion procedure and iliac fixation (thoracolumbar fusion procedures extended to sacrum are eligible in the study); * Insertion of at least 1 iFuse-3D implant according to the iFuse Bedrock technique (uni- and bilateral insertion are eligible); * Subject who preoperatively responded positively to pain provocation tests for SIJ dysfunction with or without a positive SIJ infiltration test; * Patient with a degenerative sacroiliac joint disease requested a fusion procedure; Exclusion Criteria: * Major osteoporosis (DEXA scan \> 3); * Any previous history of sacroiliac joint fusion or any surgical procedure involving a S2-iliac fusion; * Subjects requested a SIJ fusion without the iFuse-3D device or iFuse-3D not inserted according to the manufacturer instruction (Bedrock technique); * Subjects with a medical or surgical contraindication preventing the intervention from being performed or potentially interfering in the interpretation of the data collected (neurologic condition, local or systemic infection, any known allergy to surgical implants, psychiatric diseases, ...); * Currently pregnant or planning pregnancy; * Prisoner or a ward of the state; * Subject no willing to participate in the study; * Subject not affiliated to a social security insurance.