3 results
Approved WMORecruiting
European registry of children and patients with congenital heart disease that undergo ICD or CRT implantation. This will lead to a larger amount of data leading to increased knowledge about long-term consequences and potential complications.
Not approvedWill not start
To better understand the utilities of the new BETACONNECT device and characterize its contribution to adherence, we plan to prospectively follow-up MS patients using the device for 24 weeks.
Approved WMORecruiting
The aim of this study is to collect data to confirm clinical safety and performance of the Amvia pacemaker family to fulfil the regulatory requirements for products that are available on the market. The collected data may also be used to support…