RecruitingNCT06827262
Intracept Minimally-invasive PROcedure for VErtebrogenic Back Pain
Sponsor
Boston Scientific Corporation
Enrollment
1,500 participants
Start Date
Mar 26, 2025
Study Type
OBSERVATIONAL
Conditions
Summary
Compile real-world outcomes of commercially approved Intracept™ Intraosseous Nerve Ablation Systems in the treatment of patients diagnosed with vertebrogenic pain.
Eligibility
Min Age: 18 Years
Inclusion Criteria2
- 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 Criteria1
- Meets any contraindications per locally applicable Instructions for Use (IFU).
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Interventions
DEVICEIntracept™ Intraosseous Nerve Ablation
Intracept™ Intraosseous Nerve Ablation for treatment of patients diagnosed with vertebrogenic pain
Locations(15)
View Full Details on ClinicalTrials.gov
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NCT06827262
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