Severe Tricuspid Regurgitation
Conditions
Brief summary
The purpose of this study is to assess the efficacy and safety of implanting an Edwards Sapien XT Valve into the vena cava inferior (VCI; between right atrium and the hepatic vein) on clinical variables, exercise tolerance and well being in patients with severe tricuspid regurgitation and signs of right heart failure.
Interventions
DEVICEEdwards Sapien XT Valve
The device will be implanted in the present study to prevent abdominal venous congestion and to improve the function of the tricuspid valve which is located in the low pressure system in the right heart.
Sponsors
Edwards Lifesciences
Charite University, Berlin, Germany
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Severe symptomatic tricuspid regurgitation with a significant regurgitation jet into the caval and hepatic veins * Optimal medical treatment * High surgical risk with STS Score ≥ 10 or logistic EuroSCORE I ≥ 15 or any contraindication for conventional valve replacement/repair * NYHA class of at least II * Written informed consent
Exclusion criteria
* VCI diameter \> 32 mm * Severe left ventricular dysfunction with LVEF \< 30% * Severe mitral insufficiency * Estimated life expectancy \< 12months (360 days) due to carcinoma, chronic liver disease, chronic renal disease or chronic end stage pulmonary disease * Evidence of an acute myocardial infarction ≤ 1 month before the intended treatment * Evidence of stroke / TIA during the last 180 days * Leukopenia (WBC \< 3000 cell/mL), anemia (Hgb \< 9 g/dL), Thrombocytopenia (Plt \< 50,000 cells/mL), or any known blood clotting disorder * Evidence of an intracardiac mass, thrombus or vegetation * Active upper GI bleeding within 1 month (30 days) prior to procedure * Patients with an acute emergency * Contraindication or hypersensitivity to all anticoagulation regimens, or inability to be anticoagulated for the study procedure * Allergy against the use of implanted stent / prosthesis * Patient undergoing regular dialysis or a serum creatinine above 3.0 mg/dl * Patients unsuitable for implantation because of thrombosis of the lower venous system or vena cava filter * Active bacterial endocarditis within 6 months (180 days) of procedure. * Women of childbearing potential without highly effective contraception (PEARL-Index \< 1%) * Inability to comply with all of the study procedures and follow-up visits * Subjects who are legally detained in an official institute (according to § 20 MPG)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Maximum relative VO2 uptake | at 3 month | we consider the difference of means in maximum relative VO2 uptake at 3 months compared to control group. |
Secondary
| Measure | Time frame |
|---|---|
| ventilation efficiency (as assessed by the VE / VCO2 slope in spiroergometry) | day 30 and month 3 |
| Unscheduled rehospitalization | day 30 and month 3 |
| Dyspnoea VAS | day 30 and month 3 |
| Minnesota Living with Heart Failure Questionnaire | day 30 and month 3 |
| 6-minutes walk test | day 30 and month 3 |
| tricuspid regurgitation jet velocity time integral (as assessed by Doppler echocardiography) | day 30 and month 3 |
| aerobic threshold (assessed by spiroergometry) | day 30 and month 3 |
| ejection fraction (EF) | day 30 and month 3 |
| right ventricular (RV) diameter | day 30 and month 3 |
| right atrial (RA) diameter | day 30 and month 3 |
| hepatic vein diameter | day 30 and month 3 |
| N-terminal pro Brain Natriuretic Peptide (NT-proBNP) | day 30 and month 3 |
| NYHA class | day 30 and month 3 |
Countries
Germany
Outcome results
None listed