Product Surveillance Registry (PSR)

Clinical Trial Details

PSR

Product Surveillance Registry (PSR)

Purpose/Objective

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Full Trial Details: ClinicalTrials.gov

Condition: Heart Rhythm Disease
Study Type: Non-interventional
Phase: N/A
Study Start Date: 01/02/2012
Study Completion Date: 12/31/2021

The purpose of the Registry is to provide continuing evaluation and periodic reporting of safety and effectiveness of Medtronic market-released products. The Registry data is intended to benefit and support interests of patients, hospitals, clinicians, regulatory bodies, payers, and industry by streamlining the clinical surveillance process and facilitating leading edge performance assessment via the least burdensome approach.

NCT Number
NCT01524276
Principal Investigator(s)
Sean Beinart, MD
Sponsor(s)
Medtronic
Participant Eligibility
  • Age: No Minimum - No Maximum
  • Gender: Male, Female

Location

  • Adventist HealthCare White Oak Medical Center
    11890 Healing Way
    Silver Spring, MD 20904
    Main: 240-637-4000

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