Invasive Hemodynamics and Risk Stratification in T-TEER: Moving Beyond ESC Thresholds - EuroTR Registry Insights.
Giulia Masiero, Federico Arturi, Sara Ceni...
https://pubmed.ncbi.nlm.nih.gov/41235431/Actively Recruiting
Led by LMU Klinikum · Updated on 2024-03-15
3000
Participants Needed
1
Research Sites
N/A
Total Duration
Researchers are studying patients with tricuspid regurgitation, a heart valve condition linked to heart failure and high health risks. The study aims to observe clinical and survival outcomes after patients receive transcatheter tricuspid valve repair or replacement. This approach offers a new option for patients who face high risks with traditional surgery. Participants receive treatment using one of several transcatheter devices designed for tricuspid valve repair or replacement, including PASCAL, TriClip, TricValve, Evoque, or LuX-Valve. This is an observational registry collecting data in real-world settings to help improve patient selection and treatment quality for these procedures. During the study, participants will be monitored for up to five years to measure outcomes such as overall survival, technical success of the procedure, safety, heart failure markers, symptom improvement, heart function and size, valve function, and hospitalizations. This long-term follow-up will provide important information on how patients fare after these minimally invasive valve treatments.
CONDITIONS
European Registry of Transcatheter Repair for Tricuspid Regurgitation
J
Jörg Hausleiter, Prof. Dr.
L
Lukas Stolz, Dr.
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LMU Klinikum
Lead Sponsor
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Procedural period
Participants undergo transcatheter tricuspid valve repair or replacement using devices such as PASCAL or TriClip.
1 procedure visit (in-person)
Duration - Up to 5 years
Participants are monitored for clinical and survival outcomes after the device implementation.
Periodic follow-up visits over 5 years
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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Giulia Masiero, Federico Arturi, Sara Ceni...
https://pubmed.ncbi.nlm.nih.gov/41235431/LMU Klinikum
Lead Sponsor