Prevention of Postoperative Hernias in Emergency Surgery
Condition(s) studied
Study summary
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
Primary outcome measure(s)
- Incisional hernia — From the moment of inclusion until one year from the date of surgery.
Occurrence of postoperative abdominal hernia in the incision line. - Port-site hernia — From the moment of inclusion until one year from the date of surgery.
Occurrence of port-site hernia after laparoscopy. - Parastomal hernia — From the moment of inclusion until one year from the date of surgery.
Occurrence of a parastomal hernia after open/laparoscopic stoma formation
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Department of General Surgery, St Alexander Hospital | Kielce | Poland | Recruiting |
More Jan Kochanowski University trials in Poland
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06815822 on ClinicalTrials.gov ↗ ← All trials in Poland