U.S., July 30 -- ClinicalTrials.gov registry received information related to the study (NCT07092267) titled 'Safety and Efficacy Evaluation of ArtiFix(R) Sealant Graft in Subjects Requiring Dural Repair Following Neurosurgery' on July 01.
Brief Summary: The purpose of this clinical study is to evaluate and establish the safety and efficacy of the ArtiFix(R) device in subjects scheduled for cranial or spinal surgery that requires Dural defect repair (membrane that covers the brain and spinal cord). The investigated device will be implanted during the neurosurgical procedure and the participants will be asked to arrive to follow up evaluation visits at 30, 120 and 330 days post procedure.
Study Start Date: Nov., 2025
Study Type: INTERVENTI...