3 results
The objective of the International Hernia Mesh Registry is to observe a minimum of 3,500 patients for up to 2 years post implantation, in a post-market setting, following the use of either ETHICON Mesh Products or other marketed mesh products to…
The purpose of this study is to determine the safety and efficacy of post-surgery treatment with the monoclonal antibody ipilimumab, to see whether treatment improves recurrence-free survival (RFS), overall survival and distant metastases-free…
The primary objective of this study is to establish the safety and effectiveness of the WATCHMAN TM Left Atrial Appendage Closure (LAAC) Device including the post-implant medication regimen for subjects with non-valvular atrial fibrillation who are…