🏛️ Verified NIH Record • Updated 2026-04-07
Intracept Intraosseous Basivertebral Nerve Ablation (NCT05660512)
🔵 Active, Not Recruiting Interventional Protocol 📊 Observational Clinical Research Sponsor: University of Utah
🩺 Plain-English Summary (8th-Grade Level)
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.
Who can join: To join this study, participants generally need to meet the listed inclusion criteria (2 items) and avoid the listed exclusions (3 items).
Location: University of Utah Farmington Health Center — Farmington, Utah
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistCheck every box below. If you can check all of them, you may meet the study's basic screening requirements (final eligibility is confirmed by the site team).
Usually NOT eligible if any of the following apply:
- Exclusion Criteria:
- Not scheduled for an intraosseous basivertebral nerve ablation with the Intracept Procedure
- Intracept procedure for different location other than low back pain
🔍 Extracted verbatim from the official NIH eligibility criteria. Always confirm with the study coordinator.
📍 All Participating Trial Locations (3 Sites)
- University of Utah Farmington Health Center — Farmington, Utah
- University of Utah Orthopaedic Center — Salt Lake City, Utah
- University of Utah South Jordan Health Center — South Jordan, Utah
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.