Radiofrequency (RF) Ablation Prospective Outcomes Study

  • STATUS
    Recruiting
  • End date
    Mar 16, 2025
  • participants needed
    1500
  • sponsor
    Boston Scientific Corporation
Updated on 16 July 2021
Investigator
Alexander Chernyak
Primary Contact
Quincy Medical Group (1.8 mi away) Contact
+7 other location

Summary

The objective of this study is to compile real-world outcomes of Boston Scientific commercially approved radiofrequency (RF) ablation systems in the treatment of patients diagnosed with pain.

Details
Condition Chronic Pain, chronic pains
Treatment Radiofrequency ablation
Clinical Study IdentifierNCT04673032
SponsorBoston Scientific Corporation
Last Modified on16 July 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Study candidate is scheduled to be treated with a commercially approved Boston Scientific RF system for pain 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
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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