Intracept Intraosseous Basivertebral Nerve Ablation

NCT05660512 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 150

Last updated 2026-04-13

No results posted yet for this study

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.

Conditions

  • Low Back Pain

Interventions

PROCEDURE

Intracept Procedure

Radiofrequency ablation of the basivertebral nerve for the relief of chronic vertebrogenic low back pain

Sponsors & Collaborators

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-07-27
Primary Completion
2026-02-05
Completion
2026-07-31

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05660512 on ClinicalTrials.gov