A Study to Evaluate the Feasibility and Safety of the Millipede Transcatheter Annuloplasty Ring System in Patients with Functional Mitral Regurgitation
Millipede Transcatheter Annuloplasty Ring System in Patients with Functional Mitral Regurgitation
Sponsor: Boston Scientific Corporation
Enrolling: Male and Female Patients
Clinic Visits: 8
IRB Number: AAAT5421
U.S. Govt. ID: NCT04147884
Contact: Kate Dalton: 347-514-3366 / keb2114@cumc.columbia.edu
Additional Study Information: The Millipede Feasibility Study is a prospective, open-label, single-arm study to assess the safety and feasibility of the Millipede Transcatheter Annuloplasty Ring System in subjects with functional mitral regurgitation. The Millipede Annuloplasty Ring System is a novel transcatheter, fully adjustable, complete annuloplasty repair device for the treatment of mitral regurgitation. The device is designed to mimic a widely used surgical intervention with a percutaneous therapy. As such, it potentially offers a less invasive and safer treatment for mitral regurgitation in comparison to surgery. The purpose of this study is to evaluate the feasibility and safety of the Millipede Annuloplasty Ring System in patients with functional mitral regurgitation
This study is closed
Investigator
Susheel Kodali, MD
Do You Qualify?
Are you 18 years of age or older? Yes No
Have you had a prior closure of an Atrial septal defect (ASD) or patent formane ovale (PFO)? Yes No
Do you have COPD requiring continuous oxygen use? Yes No
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You may be eligible for this study

Place Holder




For more information, please contact:
Kate Dalton
keb2114@cumc.columbia.edu
347-514-3366