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An Observational Real-world Study Evaluating Severe Tricuspid Regurgitation Patients Treated With the Abbott TriClip™ Device (bRIGHT) — bRIGHT  

Tricuspid Valve Regurgitation Clinical Trial

Official title:
An Observational Real-world Study Evaluating Severe Tricuspid Regurgitation Patients Treated With the Abbott TriClip™ Device

Clinical Trial Summary

The bRIGHT EU PAS study is an observational real-world study evaluating severe tricuspid regurgitation patients treated with the Abbott TriClip™ device (bRIGHT EU Post-Approval Study).

Clinical Trial Description

The TriClip™ bRIGHT EU post-approval study (PAS) study is designed to confirm the safety and performance of the TriClip™ device in a contemporary real-world setting. The bRIGHT PAS study is a prospective, single arm, open-label, multi-center, post market registry, conducted to satisfy condition of CE Marking for the TriClip™. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04483089
Study type Observational
Source Abbott Medical Devices
Contact
Status Active, not recruiting
Phase
Start date August 27, 2020
Completion date January 2028
View Details
See also
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