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Cardiovascular Research Institute of Kansas, LLC | Wichita, KS

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Active trials

27 of 38 total trials

ALLIANCE AVIV: Safety and Effectiveness of the SAPIEN X4 Transcatheter Heart Valve in Failing Aortic Bioprosthetic Valves

The objective of this study is to establish the safety and effectiveness of the Edwards SAPIEN X4 Transcatheter Heart Valve (THV) in subjects who are...

Enrolling
Aortic Valve Stenosis
Aortic Valve Insufficiency
Device: SAPIEN X4 THV

The objective of this study is to establish the safety and effectiveness of the Edwards SAPIEN X4 Transcatheter Heart Valve (THV) in subjects with sy...

Active, not recruiting
Aortic Stenosis, Severe
Device: SAPIEN X4 THV

The objective of this trial is to evaluate the safety and effectiveness of the Amulet LAA occluder compared to NOAC therapy in patients with non-valv...

Enrolling
Atrial Fibrillation
Stroke
Drug: Non-Vitamin K Oral Antagonists
Device: Left Atrial Appendage Occlusion (Amplatzer Amulet LAA Occluder)

The purpose of this single arm, multi-center study is to confirm the safety and effectiveness of the AMPLATZER™ PFO Occluder in the post Approval Set...

Active, not recruiting
Stroke
Patent Foramen Ovale
Device: AMPLATZER™ PFO Occluder

The Amulet™ device will be evaluated for safety and efficacy by demonstrating its performance is non-inferior to the commercially available WATCHMAN®...

Active, not recruiting
Stroke
Device: WATCHMAN Left Atrial Appendage Closure
Device: Amulet Left Atrial Appendage Occluder

The objective of this study is to evaluate the preliminary safety and effectiveness of the Cephea Mitral Valve System for the treatment of symptomati...

Enrolling
Mitral Regurgitation
Device: Cephea Mitral Valve System

Prospective, randomized, open-label, international, multi-center clinical study to evaluate the safety and efficacy of the AccuCinch Ventricular Rest...

Enrolling
Heart Failure with Reduced Ejection Fraction (HFrEF)
Dilated Cardiomyopathy
Device: AccuCinch Ventricular Restoration System
Drug: Guideline-Directed Medical Therapy

Prospective, controlled, multicenter clinical investigation with four trial cohorts: Randomized, Non-repairable, Severe Mitral Annular Calcification...

Enrolling
Heart Valve Diseases
Degenerative Mitral Valve Disease
Device: Tendyne Mitral Valve System
Device: MitraClip System

Aortix is a circulatory support device for chronic heart failure patients on medical management who have been hospitalized for acute decompensated he...

Enrolling
ADHF
Heart Failure, Diastolic
Device: Aortix System

This study will evaluate the safety and effectiveness of the Edwards SAPIEN 3/SAPIEN 3 Ultra Transcatheter Heart Valve (THV) compared with clinical s...

Active, not recruiting
Aortic Stenosis, Severe
Heart Diseases
Device: Edwards SAPIEN 3 / SAPIEN 3 Ultra THV

To establish the safety and effectiveness of the Edwards PASCAL Transcatheter Valve Repair System in patients with degenerative mitral regurgitation...

Enrolling
Degenerative Mitral Valve Disease
Functional Mitral Regurgitation
Device: Edwards PASCAL System
Device: Abbott Mitraclip System
Locations recently updated

To demonstrate the safety and effectiveness of the Reducer system for treatment of patients with refractory angina pectoris treated with maximally to...

Enrolling
Refractory Angina
Other: Arm 2 (control): Implantation procedure with no device implanted
Device: Arm 3 (unblinded, non-randomized): Single arm registry

The study is an early feasibility study to measure individual patient clinical outcomes and effectiveness, evaluate the safety and function of the DU...

Enrolling
Heart Valve Diseases
Tricuspid Valve Insufficiency
Device: DUO Transcatheter Tricuspid Coaptation Valve System

The objective of ENVISION is to evaluate the safety and effectiveness of the Navitor Transcatheter Aortic Valve Implantation (TAVI) System for treati...

Invitation-only
Heart Valve Diseases
Aortic Valve Stenosis
Device: Navitor Transcatheter Aortic Valve Implantation (TAVI) System
Device: Any Commercially Available Transcatheter Aortic Valve (CAV) System

This study will monitor the safety and valve performance of the Edwards CENTERA Transcatheter Heart Valve (THV) System in patients with symptomatic,...

Active, not recruiting
Aortic Valve Stenosis
Device: TAVR with CENTERA THV

The purpose of this study is to assess if using the Impella® CP (or Impella® 2.5) device during high-risk PCI in patients with reduced left-sided hea...

Enrolling
Coronary Artery Disease
Left Ventricular Dysfunction
Device: Impella CP® / Impella CP® with SmartAssist® / Impella 2.5®
Device: IABP Intra-aortic balloon pump

The objective of this randomized controlled trial (RCT) is to compare the clinical outcome of MitraClip™ device versus surgical repair in patients wi...

Enrolling
Mitral Valve Regurgitation
Device: MitraClip™ device implantation
Procedure: Mitral Valve Repair Surgery

To establish the safety and effectiveness of the Edwards SAPIEN 3 Transcatheter Heart Valve (THV) in patients with severe, calcific aortic stenosis w...

Active, not recruiting
Aortic Stenosis
Procedure: SAVR
Device: SAPIEN 3 THV

The purpose of this clinical study is to evaluate the acute safety and effectiveness of the next-generation Navitor (Portico™ NG) Transcatheter Aorti...

Active, not recruiting
Symptomatic Severe Aortic Stenosis
Device: Portico™ NG (Navitor) Valve and FlexNav™ Delivery System
Device: Navitor Titan Valve (35mm) Valve and Large FlexNav™ Delivery System

The objective of the PORTICO pivotal IDE trial is to evaluate the safety and effectiveness of the St Jude Medical (SJM) Portico Transcatheter Heart V...

Enrolling
Aortic Valve Stenosis
Device: Portico transcatheter aortic valve
Device: Commercially available transcatheter aortic valve

Trial sponsors

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