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Clinical Trial Summary

This post-approval study (PAS) is designed to provide continued clinical evidence to confirm the long-term safety and effectiveness of the FlexAbilityTM Ablation Catheter, Sensor EnabledTM (FlexAbility SE) for the treatment of ventricular tachycardia in a post-market environment. This is a prospective, single arm, open-label, multi-center, observational study.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05839873
Study type Observational
Source Abbott Medical Devices
Contact George Galoussian
Phone 8182945677
Email george.galoussian@abbott.com
Status Recruiting
Phase
Start date July 24, 2023
Completion date November 2028

See also
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