About this trial

This is a multi-center, prospective, observational study designed to evaluate the impact of LV myocardial fibrosis extent assessed by CMR on LV reverse remodeling and clinical outcomes post TEER. The target sample will be up to 125 patients enrolled to achieve 100 evaluable at 6 months of follow-up. Enrollment will occur at up to eight centers.

Eligibility criteria

Qualifiers

None

Disqualifiers

Concomitant PCI and TEER

Congenital heart disease

Stage D heart failure

Uncontrolled atrial fibrillation

Trial design

Treatments tested in this trial

  • Cardiac MRI

Treatment groups

125 Participants
are divided into 1 treatment group

Locations

6
Italy
IRCCS Ospedale San Raffaele20132, Milan Italy
United States
Minneapolis Heart Institute Foundation55407, MinneapolisMinnesota, United States
Sanger Heart and Vascular Institute28204, CharlotteNorth Carolina, United States
The Christ Hospital Health Network45219, CincinnatiOhio, United States

Sponsors and collaborators

Minneapolis Heart Institute Foundation

Lead sponsor