Product Surveillance Registry (NCT01524276)
Medtronic Product Surveillance Registry
🩺 Plain-English Summary (8th-Grade Level)
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.
Who can join: Review the eligibility criteria below.
Location: Clinical Research Facility — Birmingham, Alabama
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (400 Sites)
Showing the first 25 of 400 sites.
- Clinical Research Facility — Birmingham, Alabama
- Clinical Research Facility — Huntsville, Alabama
- Clinical Research Facility — Chandler, Arizona
- Clinical Research Facility — Phoenix, Arizona
- Clinical Research Facility — Little Rock, Arkansas
- Clinical Research Facility — Aliso Viejo, California
- Clinical Research Facility — Chula Vista, California
- Clinical Research Facility — Colton, California
- Clinical Research Facility — La Jolla, California
- Clinical Research Facility — Los Angeles, California
- Clinical Research Facility — Napa, California
- Clinical Research Facility — Redwood City, California
- Clinical Research Facility — Salinas, California
- Clinical Research Facility — San Diego, California
- Clinical Research Facility — Stanford, California
- Clinical Research Facility — Torrance, California
- Clinical Research Facility — Ventura, California
- Clinical Research Facility — Aurora, Colorado
- Clinical Research Facility — Colorado Springs, Colorado
- Clinical Research Facility — Lakewood, Colorado
- Clinical Research Facility — Darien, Connecticut
- Clinical Research Facility — Hartford, Connecticut
- Clinical Research Facility — New Haven, Connecticut
- Clinical Research Facility — Washington D.C., District of Columbia
- Clinical Research Facility — Bradenton, Florida
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
Explore by condition: All Cardiac Rhythm Disorders clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Review the official NIH record below to find the coordinating site.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.