U.S., Sept. 3 -- ClinicalTrials.gov registry received information related to the study (NCT07800923) titled 'Long-term Follow-up of Actifit(R) Meniscal Scaffold Patients.' on July 28.
Brief Summary: This study will collect retrospective patient data of Actifit patients (medial and lateral, isolated cases as well as cases with concomitant procedures), including pre-op and any post-op imaging, for 120 retrospective Actifit patients, to account for drop-outs and patients refusing a follow-up visit/follow-up imaging.
Each patient without evidence of previous removal of the scaffold, revision to arthroplasty or joint-modifying surgery at the index knee will be contacted by the site, first by phone, to check whether the Actifit device is still ...