The ReChord Trial
Randomized Trial of the NeoChord DS1000 System versus Open Surgical Repair
The objective of this study is to assess the safety and effectiveness of the NeoChord DS1000 System in subjects with degenerative mitral valve disease. The study is designed as a randomized controlled trial comparing use of the study device versus Open Surgical Repair.
Additional information regarding the US Pivotal IDE Study may be found at www.clinicaltrials.gov.
The AcChord Study
A post‐market effectiveness registry of the NeoChord Artificial Chordae Delivery System
The objective of this study is to further describe the performance of the NeoChord DS1000 System in a post-market setting. The study is a prospective, multi-center, non-randomized design including isolated NeoChord procedures and combination valve repair procedures using the NeoChord DS1000 System and other commercially available beating heart mitral valve repair technologies.