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Radiofrequency (RF) Ablation Prospective Outcomes Study for Central Nervous System - RAPID for CNS

NCT06553625 · Boston Scientific Corporation
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Official title
Radiofrequency (RF) Ablation Prospective Outcomes Study for Central Nervous System
About this study
The objective of this study is to compile real-world outcomes of Boston Scientific Corporation commercially approved radiofrequency (RF) ablation systems used in the central nervous system (CNS) for use in functional neurosurgery.
Eligibility criteria
Inclusion Criteria: * Study candidate is scheduled to be treated with a commercially approved Boston Scientific RF system for pain or for CNS applications per local Directions for Use (DFU) * Signed a valid, IRB/EC/REB-approved informed consent form Exclusion Criteria: * Meets any contraindications per locally applicable Directions for Use (DFU) * Currently diagnosed with cognitive impairment, or exhibits any characteristic, that would limit study candidate's ability to assess pain relief or to complete study assessments
Study design
Enrollment target: 200 participants
Age groups: child, adult, older_adult
Timeline
Starts: 2024-01-29
Estimated completion: 2035-12
Last updated: 2026-07-06
Interventions
Device: Radiofrequency Ablation
Primary outcomes
  • Change in patient's quality of life (QoL) during the study as compared with baseline (Up to 24-Months)
Sponsor
Boston Scientific Corporation · industry
Contacts & investigators
ContactStephanie Delvaux · contact · BSNClinicalTrials@bsci.com · 855-213-9890
ContactDiane Keesey · contact · BSNClinicalTrials@bsci.com · 855-213-9890
InvestigatorNatalie M Bloom Lyons, M.A. · study_director, Boston Scientific Corporation
All locations (4)
Uniklinik KölnRecruiting
Cologne, Germany
Universitaetsklinikum DusseldorfRecruiting
Düsseldorf, Germany
Universitaetsklinikum WuerzburgRecruiting
Würzburg, Germany
St. Georges HospitalRecruiting
London, United Kingdom
Radiofrequency (RF) Ablation Prospective Outcomes Study for Central Nervous System - RAPID for CNS · TrialPath