Clinical Trial

A One-year Follow-up of Incisional Hernia Formation Between Device Assisted and Manual Laparotomy Closure

Recruiting
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Summary
The study compares one-year incisional hernia formation between two cohorts of patients that underwent open surgery for colorectal diseases. The patients had the abdominal wall closure performed with either a device for standardized closure or manual closure. The devices aims to secure the closure technique that is advocated by guidelines and could potentially reduce abdominal wall complications. Upholding closure quality can be cumbersome and time consuming and hence inferior closure can sometimes be associated with manual closure. Follow-up will include short term complications like wound infection and burst abdomen and one-year follow-up include a review of patients chart and CTscans performed as part of standard clinical practice.
Trial Details
NCT Number NCT07766044
Lead Sponsor Suturion AB
Collaborators: Lund University, Region Skåne Sweden
Conditions Incisional Hernia After Midline Laparotomy, Colorectal Cancer
Enrollment 218 participants
Start Date 2026-07-18
Primary Completion 2026-10-30 (estimated)
Study Completion 2026-12-30 (estimated)
Updated on ClinicalTrials.gov 2026-08-14