U.S., Dec. 20 -- ClinicalTrials.gov registry received information related to the study (NCT07295379) titled 'LIQUIBAND FIX8(R) for Ventral Incisional Hernia' on Dec. 08.
Brief Summary: This study is designed to evaluate the safety and performance of device LiquiBand FIX8 Open hernia mesh fixation device. The use of this device is not experimental, as it is already approved for use in the EU (CE-marked). This is a retrospective post market clinical follow-up study to collect information about the use of the device in a real-world setting for ventral incisional hernia repair. Ventral incisional hernias occur following surgery and the most common method of treatment includes implanting a mesh, which in the case of ventral incisional hernia, t...