Not yet recruitingObservationalLast updated Aug 11, 2026

A Registry Study to Assess SYNTHECELTM Dura Repair

SYNTHECELTM Dura Repair Registry

Overview

ClinicalTrials.gov ID: NCT07758790
Lead Sponsor: DePuy Synthes Products, Inc.INDUSTRY
Brief Summary: The purpose of this study is to assess how safe synthecel dura repair is and how well it performs in participants undergoing cranial surgery requiring dura repair (a procedure to close and protect the outer covering of the brain) in a regular, everyday healthcare environment.
Study Type

Status

Study Record Dates

NCT00859508Completed

Study of SyntheCelTM Dura Replacement to Other Dura Replacements

NCT04057157Completed

Post-market Assessment of Biodesign Dural Repair Grafts

NCT06419855Terminated

Study to Evaluate the Effectivity and Safety of BIOSCAFF®H Compared to DuraGen®, in Patients Undergoing Dural Repair

NCT07217132Not yet recruiting

Clinical Investigation Plan - Post-market Clinical Follow-up Study Collagen Dura Membrane - Suturable

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Immiseal™ Dural Sealant Post-Market Registry Study

NCT02129114Unknown status

Study to Evaluate the Safety and Efficacy of Dural Repair Patch in Neurosurgical Repairs