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Clinical Trial Summary

The purpose of this registry is to evaluate the safety and effectiveness of LBBA pacing/sensing in patients already implanted with the Tendril STS 2088 lead.


Clinical Trial Description

This registry is a retrospective, observational, non-controlled chart review conducted to support an indication expansion of the Tendril STS 2088 lead to include pacing/sensing in the left bundle branch area. Data from a minimum of 220 attempted subjects will be included in order to have 190 evaluable subjects in this registry. The chart review will be conducted at up to 20 participating centers worldwide. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05887323
Study type Observational
Source Abbott Medical Devices
Contact
Status Active, not recruiting
Phase
Start date April 25, 2023
Completion date March 31, 2024

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