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https://carolinashealthcare.org.coveo.com

Tracking Medtronic Device Results

Study Leader

Erin Murphy, MD


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    About This Study

    The purpose of this study is to collect information on how Medtronic devices work over time. We want to improve the safety and performance of these devices. The study is for volunteers who has or is intended to receive or be treated with, an eligible Medtronic product. The study team will provide more information.

    What Activities Are a Part of this Study?

    • Informed Consent Review
    • After Study Follow-Up Activities
    • Review of Medical History
    • Study Visits and Consultations

    Age & Gender

    • 18 - 100 years old
    • All Genders

    Language

    • This study enrolls English speakers only

    Additional Study Information

    • No compensation provided
    • No reimbursement offered

    Study Locations

    • Greater Charlotte, NC

    Study Topics

    Study Locations and Contacts

    • Greater Charlotte, NC: Yaritza De Los Santos Yaritza.DeLosSantos@atriumhealth.org
    • Study Information
    • IRB Number: IRB00112196

    Helpful Information

    Have questions? See if your question is answered in our most common question and answers section. Need to know what something means? Browse the dictionary for explanation of common clinical study terms.

    FAQs Dictionary


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