Radiofrequency Ablation: Radiofrequency Ablation used in the central nervous system (CNS) in functional neurosurgery
Study summary
The objective of this study is to compile real-world outcomes of Boston Scientific commercially approved radiofrequency (RF) ablation systems used in the central nervous system (CNS) for use in functional neurosurgery.
Eligibility
Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
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
Primary outcome measure(s)
Change in patient's quality of life (QoL) during the study as compared with baseline — Up to 24-Months Change in quality of life assessments during the study as compared with baseline
Trial sites (4)
Facility
City
Region
Status
Uniklinik Köln
Cologne
Germany
Recruiting
Universitaetsklinikum Dusseldorf
Düsseldorf
Germany
Recruiting
Universitaetsklinikum Wuerzburg
Würzburg
Germany
Recruiting
St. Georges Hospital
London
United Kingdom
Recruiting
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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