About this trial

The aim of this observational study is to understand the risk factors and incidence of postoperative hernias among patients undergoing emergency surgery. The main question it aims to answer is:

What is the incidence of postoperative hernias in this group of patients?

A brief telephone interview will be conducted with participants who will be included in this study one year after the surgery. If the presence of a postoperative hernia is suspected, the patient will be invited to a follow-up visit to the surgical clinic, where the diagnosis will be confirmed by imaging tests.

Eligibility criteria

Qualifiers

Patient age > 18 years.

Emergency or urgent surgery.

Specific surgical indications (acute appendicitis, acute cholecystitis, incarcerated hernia, gastrointestinal perforation, and obstruction).

Disqualifiers

Lack of patient consent.

Open abdomen technique applied.

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

500 Participants
are grouped into 2 trial groups

Locations

1
Department of General Surgery, St Alexander Hospital25-316, Kielce Poland

Sponsors and collaborators

Jan Kochanowski University

Lead sponsor