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Intracept Minimally-invasive PROcedure for VErtebrogenic Back Pain
Intracept Minimally-invasive PROcedure for VErtebrogenic Back Pain

NCT06827262

RecruitingN/A

Sponsor: Boston Scientific Corporation

Conditions: Chronic Low-back Pain, Vertebrogenic Pain Syndrome

Interventions: Intracept™ Intraosseous Nerve Ablation

Countries: United States

Compile real-world outcomes of commercially approved Intracept™ Intraosseous Nerve Ablation Systems in the treatment of patients diagnosed with vertebrogenic pain.

Eligibility overview

Sex: ALL

Age: 18 Years to

Healthy volunteers: No

Study type: OBSERVATIONAL

Eligibility criteria
Inclusion Criteria:

* Study candidate is scheduled to be treated with a commercially approved Intracept™ Intraosseous Nerve Ablation System per local Instructions for Use (IFU).
* Signed a valid, IRB/EC-approved informed consent form.

Exclusion Criteria:

* Meets any contraindications per locally applicable Instructions for Use (IFU).
Locations (19)
  • Flagstaff, Arizona, United States
  • Phoenix, Arizona, United States
  • Larkspur, California, United States
  • Westport, Connecticut, United States
  • Washington D.C., District of Columbia, United States
  • Orlando, Florida, United States
  • Jasper, Georgia, United States
  • Post Falls, Idaho, United States
  • Barrington, Illinois, United States
  • Lexington, Kentucky, United States
  • New Orleans, Louisiana, United States
  • Maple Grove, Minnesota, United States
  • Port Jefferson Station, New York, United States
  • Rochester, New York, United States
  • Bermuda Run, North Carolina, United States
  • Eugene, Oregon, United States
  • Pittsburgh, Pennsylvania, United States
  • Houston, Texas, United States
  • Salt Lake City, Utah, United States