Status: Open Not Enrolling
Investigator: Neal Kleiman
Study Coordinator: Saba Khan
Phone: 713.441.2116
This is a prospective, randomized, parallel-controlled, multicenter clinical evaluation of the MitraClip device for the treatment of clinically significant functional mitral regurgitation in symptomatic subjects too high risk to undergo mitral v ... Read more >
Status: Open Not Enrolling
Investigator: Neal Kleiman
Study Coordinator: LaShawna Green
Phone: 713.441.6548
The study is being done study to obtain data on the safety and performance of the Medtronic CoreValve® System. The Medtronic CoreValve® System has been developed to replace a diseased aortic heart valve without the need for open heart surgery. T ... Read more >
Status: Open Not Enrolling
Investigator: Neal Kleiman
Study Coordinator: LaShawna Green
Phone: 713.441.6548
The purpose of the study is to evaluate the safety and efficacy of the Medtronic CoreValve® System in the treatment of symptomatic severe aortic stenosis in subjects who have a predicted high risk for aortic valve surgery and/or very high risk f ... Read more >
Status: Enrolling
Investigator: Neal Kleiman
Study Coordinator: LaShawna Green
Phone: 713.441.6548
The primary objective of the study is to evaluate the safety and effectiveness of the Medtronic CoreValve® System (MCS) in a subset of subjects excluded from the U.S. Extreme Risk Pivotal Trial population due to one or more additional co-morbidi ... Read more >
Status: Open Not Enrolling
Investigator: Neal Kleiman
Study Coordinator: Patricia Brinegar
Phone: 713.441.3506
To evaluate the safety and efficacy of the CoreValve Evolut R System in patients with severe symptomatic aortic stenosis who are considered at high through extreme risk for surgical aortic valve replacement ... Read more >
Status: Enrolling
Investigator: Neal Kleiman
Study Coordinator: LaShawna Green
Phone: 713.441.6548
The objective of this study is to evaluate the safety and effectiveness of the Lotus™ Valve System for transcatheter aortic valve replacement (TAVR) in symptomatic subjects with calcific, severe native aortic stenosis who are considered at extre ... Read more >
Status: Enrolling
Investigator: Neal Kleiman
Study Coordinator: Jeannie Arredondo
Phone: 713.441.3574
The purpose of the study is to investigate the safety and efficacy of transcatheter aortic valve implantation (TAVI) in patients with severe, symptomatic Aortic Stenosis (AS) at intermediate surgical risk by randomizing patients to either Surgic ... Read more >
Status: Enrolling
Investigator: Neal Kleiman
Study Coordinator: Patricia Brinegar
Phone: 713.441.3506
The purpose of this study is to determine the incidence and predictors of high degree or complete atrioventricular block (AVB) (paroxysmal or persistent) in patients with new-onset persistent left bundle branch block (NOP-LBBB) following transca ... Read more >
