EP Device Registry

Launched by ABBOTT MEDICAL DEVICES · Jul 6, 2020

Keywords

ClinConnect Summary

The EP Device Registry is a clinical trial studying the safety and effectiveness of Abbott's electrophysiology devices, which are used to diagnose and treat heart rhythm disorders. The goal of this study is to gather ongoing, high-quality information about how well these devices work in real-life situations, outside of a controlled clinical environment.

To participate in this trial, you need to have had a specific heart imaging or treatment procedure using one of Abbott's devices. It's also important that you're able to follow up with your healthcare team as recommended. If you're currently involved in another clinical study that might affect the results of this registry, you won't be eligible to participate. If you join, you can expect to provide information about your experience with the device over time, helping researchers understand its benefits and safety in everyday use.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Subject underwent an electrophysiology imaging (diagnostic procedure) and/or ablation procedure that used one or more Abbott devices covered by this Registry.
• • Subject is willing and able to comply with the site's standard of care follow-up schedule.
• Exclusion Criteria:
• • Subject is currently participating in another clinical investigation that may confound the results of this Registry.