Clinical Trial: ProSpectic Italian Laparoscopic Hybrid mEsh hErnia Repair in Obese patientS Trials
Study Status: Completed
Recruit Status: RECRUITING
Condition: Uncomplicated Ventral Incisional Hernia
Study Type: OBSERVATIONAL
Official Title: Laparoscopic Ventral Hernia Repair in Obese Patients: Safe and Effective Use of a Hybrid (PTFE / Biosynthetic) Mesh. Results of a Multicentric Prospective Trial.
Brief Summary:
The aim of this study is to evaluate safety and effectiveness of a hybrid mesh (GORE® SYNECOR Intraperitoneal Biomaterial) in patients with a BMI of 30 kg/m2 or more undergoing laparoscopic ventral hernia repair (LVHR) with intraperitoneal position of the mesh.
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