Clinical trials: Implanted With Any Currently (and Any Future) FDA-approved Medtronic ICD or CRT Device
Implanted With Any Currently (and Any Future) FDA-approved Medtronic ICD or CRT Device, to Which is Attached a St. Jude Riata Lead
Insulation Failure in St. Jude Riata Leads
A recent study evaluated the Manufacturer and User Facility Device Experience (MAUDE) database, which contains reports of adverse events involving medical devices6,9. The FDA updates the database every two months.
- Trial name
- NCT02095977
- Testing
- fluoroscopy, synchronized high-voltage shock, Holter monitor
- Where
- United States
- Volunteers
- 30 people
- Sponsor
- Hartford Hospital