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Life sciences · Observational Study
ClinicalTrials.gov · November 6, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Observational Study.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
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Registry record from ClinicalTrials.gov (NCT06547138). This is a study registration, not published results. Lead sponsor: Aesculap AG. Recruitment status: NOT_YET_RECRUITING. Study type: OBSERVATIONAL. Enrollment: 110 participants (ESTIMATED). Conditions: Abdominal Aortic Aneurysm, Morbid Obesity. Interventions: DEVICE: Prophylactic mesh. Primary outcome measures: Surgical Site Infection (SSI) A2/A3 rate , at 6 months follow-up. Brief summary: The aim of the study is to describe the effectiveness of Optilene® Silver Mesh Elastic on prevention of surgical site infection (SSI) at 6 months follow-up in patients undergoing urgent laparotomy by collecting clinical data on the SSI rates, IH rates and overall clinical performance of Optilene® Silver Mesh Elastic used for the prevention of incisional hernia as prophylactic mesh in patients that require urgent median laparotomy in clinical routine.