Product Surveillance Registry (PSR)
Medtronic Product Surveillance Registry
Sponsor: Medtronic
This observational or N/A phase trial investigates Aortic, Peripheral Vascular and Venous Disorders and Cardiac Rhythm Disorders and is currently actively recruiting participants. Medtronic leads this study, which shows 53 recorded versions since 2012 — indicating substantial longitudinal coverage. Heart and vascular conditions benefit from the kind of long-term tracking this trial provides.
Status Flow
Change History
53 versions recorded-
Apr 21, 2026 — Present [daily]
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▶ Show 48 earlier versions
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Dec 2022 — Jan 2023 [monthly]
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Sep 2022 — Dec 2022 [monthly]
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Nov 2021 — Jan 2022 [monthly]
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Oct 2021 — Nov 2021 [monthly]
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Sep 2021 — Oct 2021 [monthly]
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May 2021 — Jun 2021 [monthly]
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Oct 2020 — Jan 2021 [monthly]
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Sep 2019 — Sep 2020 [monthly]
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Dec 2018 — Jul 2019 [monthly]
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Oct 2018 — Dec 2018 [monthly]
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Jun 2018 — Oct 2018 [monthly]
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Apr 2018 — Jun 2018 [monthly]
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Phase: NA → None
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Oct 2017 — Apr 2018 [monthly]
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Feb 2017 — Oct 2017 [monthly]
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Jan 2017 — Feb 2017 [monthly]
Recruiting NA
First recorded
Jan 2012
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
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.
Contact Information
- Medtronic
For direct contact, visit the study record on ClinicalTrials.gov .