A One-year Follow-up of Incisional Hernia Formation Between Device Assisted and Manual Laparotomy Closure
Recruiting · NCT07766044 · Interventional (participants receive a specific treatment) · Lead sponsor: Suturion AB
View the official record on ClinicalTrials.gov →Interventions studied
What this trial is about
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.
Who can take part
Inclusion criteria
- \>18 years of age
- Patients selected for elective surgical procedure through a midline incision due to colorectal disease
Exclusion criteria
- Previous surgery including the midline
- Previous hernia including the midline
- Collagen disease
- Disseminated disease at the time of surgery
- Life expectancy less than 1 year.
Where it is running
1 location listed.
- Helsingborg hospital - Helsingborg, Skåne County, Sweden