Medtronic Product Surveillance Registry

Medtronic Product Surveillance Registry

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PROTOCOL DESCRIPTION

The purpose of this Registry is to collect post-market surveillance data for the continuing assessment of product performance and clinical outcomes. Provide an extensive repository of "real-world" data for identification of emerging safety or performance issues. Gain a better understanding of the relationship between a product's performance and clinical outcomes.

ELIGIBILITY CRITERIA

Patients MUST:

  • Patient has or is intended to receive or be treated with an eligible product within a specified enrollment window.

Primary Investigator(s):
Jeannie Perkins

Contact Information:
Karen D. Buchanan, RN, BSN
Clinical Research Nurse
Phone: 540-984-7493
Email: kdbuchanan@carilionclinic.org