Overview
The study is designed to collect data on Cardiovascular Implantable Electronic Device (CIED) information, implant procedure details, and/or patient characteristics to support development of future CIED products and procedures.
Description
This is a data collection, non-randomized, multi-center study. The study will consist of different cohorts with each cohort being independent from another cohort. Each cohort may have a distinct objective, cohort-specific subject population, procedures, and assessments. The study will follow subjects receiving routine care, who meet all of the inclusion criteria and none of the exclusion criteria.
Eligibility
Inclusion Criteria:
- Subject is at least 18 years of age.
- Subject is willing and able to provide written informed consent.
- Subject is willing and able to complete the study procedures and visits for the duration of data collection requirements
Exclusion Criteria:
- Subject is unwilling or unable to comply with study procedures as defined in the protocol.
- Subject with a medical condition that precludes the patient from participation in the opinion of the investigator.
- Subject is enrolled in another study that could confound the results of this study, without documented pre-approval from a Medtronic study manager.