Text Size
22 studies found for:    university of kansas hospital | Open Studies | heart disease | United States, Kansas

Modify this search | How to Use Search Results

Show Display Options
Rank Status Study
1 Recruiting Adult Congenital Heart Disease Registry (QuERI)
Conditions: Pulmonary Arterial Hypertension;   Congenital Heart Disease
Intervention: Other: observational
2 Recruiting NAVISTAR® THERMOCOOL® SF Catheter: Observational Study
Conditions: Atrial Fibrillation;   Paroxysmal Arrhythmia
Intervention: Device: Catheter Ablation (NAVISTAR® THERMOCOOL® SF Catheter)
3 Recruiting Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in High Risk and Very High Risk Subjects Who Need Aortic Valve Replacement
Condition: Severe Aortic Stenosis
Interventions: Device: Medtronic CoreValve® System Transcatheter Aortic Valve Implantation (TAVI);   Device: Surgical Aortic Valve Replacement (SAVR)
4 Recruiting Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Condition: Severe Aortic Stenosis
Intervention: Device: Medtronic CoreValve® System Transcatheter Aortic Valve Implantation (TAVI)
5 Recruiting Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment of Severe, Symptomatic Aortic Stenosis in Intermediate Risk Subjects Who Need Aortic Valve Replacement (SURTAVI).
Condition: Severe Aortic Stenosis
Interventions: Device: Medtronic CoreValve® System Transcatheter Aortic Valve Implantation (TAVI);   Procedure: Surgical Aortic Valve Replacement (SAVR)
6 Recruiting Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis With Significant Comorbidities in Very High Risk Subjects Who Need Aortic Valve Replacement
Condition: Severe Aortic Stenosis
Intervention: Device: Medtronic CoreValve® System Transcatheter Aortic Valve Implantation (TAVI)
7 Recruiting nMARQ™ Pulmonary Vein Isolation System for the Treatment of Paroxysmal Atrial Fibrillation
Condition: Atrial Fibrillation
Interventions: Device: nMARQ Navigation Catheters;   Device: NaviStar ThermoCool Catheters
8 Recruiting Eisenmenger Quality Enhancement Research Initiative
Condition: Eisenmenger
Intervention: Other: Management
9 Recruiting THERMOCOOL® SMARTTOUCH™ Catheter for the Treatment of Symptomatic Paroxysmal Atrial Fibrillation CONTINUED ACCESS
Condition: Drug Refractory Symptomatic Paroxysmal Atrial Fibrillation
Intervention: Device: THERMOCOOL® SMARTTOUCH™ Catheter
10 Recruiting PRE-DETERMINE Cohort Study
Conditions: Coronary Artery Disease;   Left Ventricular Dysfunction;   Sudden Cardiac Death
Intervention:
11 Recruiting Pivotal Clinical Study of the CardioFocus Endoscopic Ablation System - Adaptive Contact (EAS-AC) (HeartLight) in Patients With Paroxysmal Atrial Fibrillation (PAF)
Condition: Paroxysmal Atrial Fibrillation
Interventions: Device: EAS-AC (HeartLight);   Procedure: Control Arm Ablation
12 Recruiting Aspirin in Reducing Events in the Elderly
Conditions: Functional Disability;   Dementia;   Heart Disease;   Stroke;   Cancer;   Bleeding
Interventions: Drug: 100 mg enteric-coated aspirin;   Drug: Placebo
13 Recruiting Acute Kidney Injury Neutrophil Gelatinase-Associated Lipocalin (N-GAL) Evaluation of Symptomatic Heart Failure Study (AKINESIS)
Conditions: Acute Decompensated Heart Failure;   Acute Kidney Injury
Intervention:
14 Recruiting Left Atrial Pressure Monitoring to Optimize Heart Failure Therapy
Condition: Heart Failure
Intervention: Device: HeartPOD™ System or Promote® LAP System
15 Recruiting VIVID - Valvular and Ventricular Improvement Via iCoapsys Delivery - Feasibility Study
Conditions: Mitral Valve Regurgitation;   Left Ventricular Dysfunction;   Heart Failure;   Mitral Insufficiency;   Mitral Incompetence;   Ischemic Heart Disease
Intervention: Device: Percutaneous mitral valve repair
16 Recruiting Insulin Resistance Intervention After Stroke Trial
Conditions: Stroke;   Myocardial Infarction;   Diabetes
Interventions: Drug: pioglitazone;   Drug: placebo
17 Recruiting AMR-001 Versus Placebo Post ST Segment Elevation Myocardial Infarction
Condition: ST Segment Elevation Myocardial Infarction
Interventions: Biological: AMR-001;   Other: placebo
18 Recruiting Randomized On-X Anticoagulation Trial
Condition: Heart Valve Disease
Interventions: Device: On-X valve using reduced anticoagulation;   Device: On-X Valve with Standard Coumadin Therapy
19 Recruiting ST Monitoring to Detect Acute Coronary Syndrome Events in Implantable Cardioverter Defibrillator Patients
Condition: Coronary Artery Disease
Intervention: Device: Fortify ST
20 Recruiting Longitudinal Surveillance Registry (LSR) of ACUITY Spiral
Condition: Heart Failure
Intervention: Device: ACUITY Spiral LV Lead
To Top

Previous Page Studies Shown (1-20) Next Page (21-22) Show next page of results
† Indicates status has not been verified in more than two years