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Clinical Trial Summary

The purpose of the Confirm Rx SMART Registry is to collect real world data to assess the safety and performance of the Confirm Rx Insertable Cardiac Monitor (ICM) and system over a 12 month period. A sub-set of subjects enrolled in the Confirm Rx SMART Registry will meet the Post Market Clinical Follow-Up (PMCF) requirement for CE mark.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03505801
Study type Observational [Patient Registry]
Source Abbott Medical Devices
Contact
Status Active, not recruiting
Phase
Start date April 24, 2018
Completion date March 31, 2026

See also
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