A One-year Follow-up of Incisional Hernia Formation Between Device Assisted and Manual Laparotomy Closure
NCT: NCT07766044 · RECRUITING
Brief 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.
Frequently Asked Questions
What is A One-year Follow-up of Incisional Hernia Formation Between Device Assisted and Manual Laparotomy Closure?
A One-year Follow-up of Incisional Hernia Formation Between Device Assisted and Manual Laparotomy Closure is a clinical trial registered under NCT07766044. Current status: RECRUITING.
What is the status of NCT07766044?
The current status of NCT07766044 (A One-year Follow-up of Incisional Hernia Formation Between Device Assisted and Manual Laparotomy Closure) is: RECRUITING.
When did A One-year Follow-up of Incisional Hernia Formation Between Device Assisted and Manual Laparotomy Closure start?
A One-year Follow-up of Incisional Hernia Formation Between Device Assisted and Manual Laparotomy Closure started on 2026-07-18.
Related Devices
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.