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Active clinical trials for "Tricuspid Valve Insufficiency"

Results 91-100 of 144

Percutaneous Treatment of Tricuspid Valve Regurgitation With the TriCinch System™

Tricuspid Regurgitation

The TriCinch System™ is intended for percutaneous treatment of tricuspid regurgitation. It is a percutaneous catheter-based device designed for tricuspid valve repair in order to decrease effective cross-sectional area and relieve symptoms in patients with tricuspid valve regurgitation.

Completed15 enrollment criteria

Comparison of Sternal Wound Infiltration With Liposomal Bupivacaine v. Bupivacaine Hydrochloride...

Coronary Artery DiseaseCoronary Artery Stenoses4 more

The aim of this study is to evaluate the analgesic efficacy and safety of wound infiltration with liposomal bupivacaine (LB) in patients undergoing cardiac surgery with sternotomy and cardiopulmonary bypass (CPB) and compare it with bupivacaine hydrochloride infiltration

Completed16 enrollment criteria

TRICUS STUDY Euro - Safety and Efficacy of the TricValve® Device

Severe Tricuspid Regurgitation

The TricValve® Transcatheter Bicaval Valves System is indicated for relief of tricuspid insufficiency in patients with symptomatic heart disease who are judged by a heart team, including a cardiac surgeon, to be at extreme risk or inoperable for open surgical therapy.

Completed29 enrollment criteria

MATTERS II - Mistral Percutaneous Tricuspid Valve Repair FIM Study

Tricuspid Valve Regurgitation

The Mistral is an investigational device intended for percutaneous trans-catheter repair in high risk for surgery individuals suffering from functional Tricuspid Regurgitation (TR). The device system is to be used only in accordance with the approved Investigational Plan on subjects who have signed an informed consent form. Device use is limited to the approved study investigators.

Completed39 enrollment criteria

Treatment of Tricuspid Valve Regurgitation in Patients Undergoing Left Ventricular Assist Device...

Tricuspid Valve InsufficiencyRight Heart Failure1 more

The purpose of this study is to determine the utility of tricuspid valve repair at the time of LVAD implantation for patients presenting with moderate or severe tricuspid regurgitation. The study will be a randomized trial for patients presenting for LVAD implantation to either tricuspid valve repair or no tricuspid valve repair. The data will be analyzed as both an intention to treat analysis as well as an "as treated" analysis with the primary outcome being rates of right ventricular dysfunction post LVAD implantation. Tricuspid valve repair for these patient is currently being done for some patients, without any strong data to either support such practice or negate it.

Completed9 enrollment criteria

Early Feasibility Study of the Edwards FORMA Tricuspid Transcatheter Repair System

Tricuspid Valve Regurgitation

The study is a multi-center, prospective, early feasibility study to measure individual patient clinical outcomes and effectiveness, evaluate the safety and function, provide guidance for future clinical study designs and development efforts of the Edwards FORMA Tricuspid Transcatheter Repair System.

Completed5 enrollment criteria

Prophylactic Tricuspid Annuloplasty During Mitral Valve Surgery

Tricuspid Valve Insufficiency

Single center randomized study to test whether a prophylactic tricuspid annuloplasty at the time of mitral valve procedure can improve clinical and echocardiographical outcomes.

Completed5 enrollment criteria

Comparison of Rigid Annuloplasty Ring With a Band in the Correction of Secondary Tricuspid Insufficiency...

Tricuspid Regurgitation

randomized study which include comparison rigid ring and band devices in treatment tricuspid regurgitation.

Completed2 enrollment criteria

"Atriogenic Tricuspid Selected, Omics Profile, Multimodality Imaging and Clinical Outcomes"

Tricuspid Valve Insufficiency

The aim of our study is to investigate the molecular mechanisms underlying remodeling of the tricuspid valve apparatus in patients with ITF and isolated AF, in comparison with patients with ITF from right ventricular remodeling, patients with atriogenic MI and left ventricular remodeling. To achieve these aims, markers obtained from cardiovascular imaging methods, such as 3D echocardiogram, and biomarkers isolated from the peripheral blood of the study participants will be considered.

Active7 enrollment criteria

Tricuspid Regurgitation Study

Tricuspid RegurgitationRight Ventricular Dysfunction1 more

The effect of cardiac pacing leads on tricuspid regurgitation is unclear. This study will determine whether using a smaller diameter leads and an alternate position in the ventricle, the proximal septum, will reduce tricuspid regurgitation than larger leads placed in the apex.

Completed12 enrollment criteria
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