Early Feasibility Study to evaluate the safety and performance of the Innoventric Trillium™ Stent Graft in the treatment of severe or greater tricuspid regurgitation (TR).
Prospective, single arm, multi-center, Early Feasibility Study (EFS) to assess the safety and performance of the Innoventric Trillium™ Stent Graft in the treatment of severe or greater tricuspid regurgitation (TR). Up to fifteen (15) patients at up to 10 US investigational sites and 3 German investigational sites will be enrolled. All enrolled study patients will be assessed at baseline, during the procedure, at discharge, and after 1 month, 3 months, 6 months, 1 year, 2 years, 3 years, 4 years, and 5 years following the index procedure.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
15
Trillium™ Stent Graft for Cross-Caval Tricuspid Valve Replacement
Cardiovascular Institute of Los Robles Health System
Thousand Oaks, California, United States
RECRUITINGAscension St. John
Detroit, Michigan, United States
Rate of Major Adverse Events [Safety endpoint]
Rate of device or procedure-related Major Adverse Events (MAEs) And Rate of unplanned surgery or re-intervention due to a life-threatening device or procedure failure
Time frame: at the end of the procedure, at discharge - typically within a week, and 30 days
Technical Performance
Successful access, delivery, and retrieval of the Trillium™ delivery system, device is anchored both in SVC and IVC \[at the end of the procedure\] And No need for re-intervention due to device valve regurgitation or para-stent leak \[at discharge, and 30 days\]
Time frame: at the end of the procedure, at discharge - typically within a week, and 30 days
Rate of Major Adverse Events [Safety endpoint]
* Composite of all device or procedure-related MAEs \[at 3 months, 6 months, 1, 2, 3, 4, and 5 years\]. * Device thrombosis, evaluated by Echocardiography \[at 30 days, 6 months, 1, 2, and 4 years\]. * Device Migration as evaluated by Echocardiography or CMR \[at 6 months\]
Time frame: at 3 months, 6 months, 1, 2, 3, 4, and 5 years
Efficacy endpoint
One or more of the following- * TR grade as measured on the device valves by Echocardiography, or reduction in peak CVP as measured by right heart catheterization \[at the end of the procedure\] * TR grade as measured on the device valves by Echocardiography \[at 30 days, 6-month, 1-year, 2-year, and 4-year\] * Rate of hospitalizations for HF \[at 6-month, and 1-year\] * HF functional class (NYHA) \[at 30 days, 3-month, 6-month,1-year, 2-year, 3-year, 4-year, and 5-year\] * Six-minute walk test (6MWT) \[at 30 days, 6-month, 1-year, 2-year, and 4-year\] * The Kansas City Cardiomyopathy Questionnaire (KCCQ) \[at 30 days, 3-month, 6-month, 1-year, 2-year, 3-year, 4-year, and 5-year\] * Patient Global Assessment (PGA) for Tricuspid Regurgitation Valve Treatment \[at 30 days, 3-month, 6-month, 1-year, 2-year, 3-year, 4-year, and 5-year\]
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Mayo Clinic Hospital (Rochester)
Rochester, Minnesota, United States
RECRUITINGWeill Cornell Medicine
New York, New York, United States
RECRUITINGStony Brook Heart Institute
Stony Brook, New York, United States
RECRUITINGThe Christ Hospital
Cincinnati, Ohio, United States
RECRUITINGLankenau Heart Institute
Philadelphia, Pennsylvania, United States
RECRUITINGTriStar Centennial Medical Center
Nashville, Tennessee, United States
RECRUITINGUniversity of Washington Medical Center
Seattle, Washington, United States
RECRUITINGUniversity Medicine Mainz
Mainz, Rhineland-Palatinate, Germany
RECRUITING...and 2 more locations
Time frame: at 30 days, 3-month, 6-month, 1-year, 2-year, 3-year, 4-year, and 5-year