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

Sponsor: Boston Scientific Corporation

NCT ID: NCT06553625

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Health checks and monitoring — no treatment given
Type of study
Observational (no treatment given)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Radiofrequency Ablation (device)
How long the study runs
Study runs about 143 months (dates as stated)
About the drug or intervention
Radiofrequency Ablation — device: Radiofrequency Ablation used in the central nervous system (CNS) in functional neurosurgery
Patient visit burden
Not specified by the sponsor
Type of study
Observing health over time
Ages
Not specified
Who
All
Number of participants
200
Started
2024-01-29
Last checked
2026-09

Plain English Summary

What is this study?

  • • Testing a new treatment for parkinson disease
  • • Clinical study - 200 participants
  • • 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

Who can take part?

  • • Adults
  • • Diagnosed with parkinson disease

Where?

  • • London - St. Georges Hospital

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

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.

More detail

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.

Parkinson DiseaseDystoniaEssential TremorMovement Disorders

How this trial compares with your answers

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What we know so far

Condition· Matched your search
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Still need:

  • • Tell us your age for better matching
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Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: Not specified
  • Who can join: All genders

What the study is looking for

  • ✓Study candidate is scheduled to be treated with a commercially approved Boston Scientific RF system for pain or for...
  • ✓Signed a valid, IRB/EC/REB-approved agreement to take part form

Who cannot take part

  • ✗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...
See the full 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

Where Is This Study? (1 UK site)

St. Georges Hospital

London, United Kingdom

Recruiting
Site contact (verified)
Boston Scientific Clinical Research855-213-9890BSNClinicalTrials@bsci.com

How to Get in Touch

Stephanie Delvaux

Sponsor contact

CONTACT

855-213-9890 BSNClinicalTrials@bsci.com

Diane Keesey

Sponsor contact

CONTACT

855-213-9890 BSNClinicalTrials@bsci.com
Data sourced from ClinicalTrials.gov · Last verified: 2026-09