Intracept Intraosseous Basivertebral Nerve Ablation

This is an independent prospective, noninterventional, observational post market data collection of the patient-reported effectiveness, ongoing safety, and satisfaction outcomes for patients treated with the Intracept Procedure at a single study site.This study will be conducted according to Good Clinical Practice (GCP) guidelines, including participant verbal informed consent and Independent Review Board (IRB) / Ethics Committee (EC) approval and oversight.Study design, conduct, analysis, and reporting are overseen by the Principal Investigator (PI) and the cross-specialty Independent Physician Steering Committee.

Inclusion Criteria:All patients scheduled for intraosseous basivertebral nerve ablation with the Intracept ProcedureExclusion Criteria:Not scheduled for an intraosseous basivertebral nerve ablation with the Intracept ProcedureIntracept procedure for different location other than low back pain