This is a single center prospective cohort study. The cohort (interventional) patients will receive the study intervention (ABCLO). The control group retrospective patients that were previously managed at the same center, regardless of the technique or the device used to close the OA.
AbCLO Open Abdomen Study
Assessment of a non-invasive device in the management of Open Abdomen – Pilot Study
Surgery, Trauma
All genders
18-99
Recruiting now
Overview
Principal Investigator: Mohammed Bawazeer
Contact Us
Stephanie Gomez
Study details
Inclusion Criteria
- 1) Adults more than 18 years of age
- 2) Admitted to the trauma and acute care surgery service, underwent damage control
laparotomy and left with an open abdomen (OA).
Exclusion Criteria
- 1) Pregnant patients
- 2) Patients who lost any portion of the abdominal wall that preclude primary abdominal wall
closure - 3) patient who previously had a ventral hernia before having an open abdomen