Product Surveillance Registry
Status: | Recruiting |
---|---|
Conditions: | Peripheral Vascular Disease, Cardiology, Neurology, Gastrointestinal, Urology, Digestive Disease |
Therapuetic Areas: | Cardiology / Vascular Diseases, Gastroenterology, Nephrology / Urology, Neurology |
Healthy: | No |
Age Range: | Any |
Updated: | 11/8/2018 |
Start Date: | January 2012 |
End Date: | January 2030 |
Contact: | Medtronic Product Surveillance Registry |
Email: | rs.productsurveillanceregistry@medtronic.com |
Medtronic Product Surveillance Registry
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.
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.
Inclusion Criteria:
- Patient or legally authorized representative provides written authorization and/or
consent per institution and geographical requirements
- Patient has or is intended to receive or be treated with an eligible Medtronic product
- Patient within enrollment window relative to therapy initiation or meets criteria for
retrospective enrollment
Exclusion Criteria:
- Patient who is, or will be, inaccessible for follow-up
- Patient with exclusion criteria required by local law
- Patient is currently enrolled in or plans to enroll in any concurrent drug and/or
device study that may confound results
We found this trial at
137
sites
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