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NCT05632952
ProSpectic Italian Laparoscopic Hybrid mEsh hErnia Repair in Obese patientS Trials
Conditions: Uncomplicated Ventral Incisional Hernia, Obesity
Sex: All
Ages: 18 Years – N/A
Enrollment: 120
Sponsor: Azienda Sanitaria Locale Napoli 2 Nord
Location: Italy
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.
Eligibility Criteria
Inclusion Criteria:age > 18 yearsClean woundsInformed consentPatients affected by Incisional and Ventral HerniaElective surgeryHernia size between 3 e 7 cmBMI > 30 kg/m2Exclusion Criteria:age < 18 years;Life expectancy < 24 months (as estimated by the operating surgeon), -PregnancyImmunosuppressant therapy within 2 weeks before surgeryClean-contaminated and contaminated, dirty woundsCirrhosis
Source: ClinicalTrials.gov (NCT05632952). StuddyBuddy aggregates publicly available trial information.
