Intracept Intraosseous Basivertebral Nerve Ablation

Running, not enrolling

Conditions studied: Low Back Pain

In brief

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.

Key facts

Study ID

NCT05660512

Run by

University of Utah

People needed

150

Starts

2020-07-27

Expected to finish

2026-07-01

Last updated by the study team

2026-04-13

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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.

You may not qualify if…

• Not scheduled for an intraosseous basivertebral nerve ablation with the Intracept Procedure
• Intracept procedure for different location other than low back pain

Where it is running

• University of Utah Farmington Health Center — Farmington, Utah, United States
• University of Utah Orthopaedic Center — Salt Lake City, Utah, United States
• University of Utah South Jordan Health Center — South Jordan, Utah, United States

Full record on ClinicalTrials.gov

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