Intracept Intraosseous Basivertebral Nerve Ablation

Launched by UNIVERSITY OF UTAH · Dec 13, 2022

Keywords

ClinConnect Summary

The Investigator Sponsor will initially approach patients planning to undergo the Intracept Procedure to discuss their interest in learning more about the study. With patient permission, contact information will be forwarded to a third-party research organization which will contact the patient to explain more about the study and to gather Verbal Informed Consent.

Study data will be collected by the University of Utah research staff via 4 telephone study visits under the direction of the Sponsor Investigator. The study research staff will enter the study data directly into a study database ...

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • All patients scheduled for intraosseous basivertebral nerve ablation with the Intracept Procedure
• • OR Participant had an Intracept Procedure for their low back pain and completed standard of care questionnaires at their procedure appointment.
• Exclusion Criteria:
• • Not scheduled for an intraosseous basivertebral nerve ablation with the Intracept Procedure
• • Intracept procedure for different location other than low back pain