Active — Not RecruitingNot Applicable

Intracept Intraosseous Basivertebral Nerve Ablation

United States150 participantsStarted 2020-07-27

Plain-language summary

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 participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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

What they're measuring

Oswestry Disability Index (ODI) Change

Timeframe: 3 months

Trial details

NCT IDNCT05660512

SponsorUniversity of Utah

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2026-02-05

View on ClinicalTrials.gov More Low Back Pain trials