Abbott Vascular Medical Device Registry

Launched by ABBOTT MEDICAL DEVICES · Sep 30, 2020

Keywords

ClinConnect Summary

The Abbott Vascular Medical Device Registry is a clinical study designed to collect and evaluate information about specific medical devices used to treat certain heart and blood vessel conditions, such as heart attacks and blood clots. The goal of this study is to ensure these devices are safe and effective throughout their use, and to identify any new risks that might arise. It is an ongoing study that is currently looking for participants.

To be eligible, you need to be at least 18 years old and have a scheduled or recent procedure that involves one of the Abbott devices included in the study. Participants will need to agree to follow a set schedule for check-ups after the procedure. It’s important to note that if you have had symptoms of COVID-19 or another contagious illness in the last two months, you may not qualify for this study. If you decide to participate, you will provide informed consent, which means you understand the study and agree to take part before any data is collected.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • 1. Subject is at least 18 years of age.
• • 2. Subject has a planned procedure, or underwent a procedure, that will use/used one or more Abbott target devices covered in this registry.
• • 3. Subject is willing and able to comply with, or has already completed, the follow-up schedule specified in this protocol.
• • 4. Subject must provide written informed consent prior to any clinical investigation-related data collection or be enrolled under an IRB/EC approved waiver of consent.
• Exclusion Criteria:
• • 1. Subject has active symptoms and/or a positive test result of COVID-19 or other rapidly spreading novel infectious agent within the prior 2 months of the date of procedure.