The first patient who was randomized to receive an Agili-C implant in the US is a 53-year-old male. He suffered from a chronic painful cartilage lesion in the trochlea’s center and received a single implant in a mini-arthrotomy approach.”Currently we lack good treatment options for patients who experience persistent knee pain due to cartilage problems and are too young for knee replacement” said Dr. Dasa. “The Agili-C implantation was smooth without complications. We plan to enroll more patients in the upcoming weeks and hope that this lDE trial finds that the Agili-C implant alleviates pain in these patients, allowing them to return to an active lifestyle.”
In Europe and Israel, 80 patients have already been enrolled and treated in the study, which will include a minimum of 250 patients in US and OUS centers, aiming for an FDA PMA application. The trial’s objective is to demonstrate the superiority of the Agili-C implant over surgical standard of care (microfracture and debridement) for the treatment of cartilage or osteochondral defects, in both arthritic knees and knees without degenerative changes.
Nir Altschuler, CartiHeal‘s founder & CEO said, “We would like to congratulate Dr. Dasa and Dr. Hartman for enrolling the first two US patients. This is a significant milestone for our company and for our study. We are very pleased with the enrollment rate to date, and plan to open more US sites in the near future.”
For more information about the Agili-C IDE study at LSU Health New Orleans, contact Cara Rowe, MSW, CCRP, Orthopaedics Clinical Research Coordinator at 504-568-4640.
CartiHeal, a privately-held medical device company with headquarters in Israel, develops proprietary implants for the treatment of cartilage and osteochondral defects in traumatic and osteoarthritic joints. In the United States the Agili-C implant is not available for sale – it is an investigational device limited for use in the IDE study.
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