Prevention of Postoperative Hernias in Emergency Surgery

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-100
SponsorJan Kochanowski University

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

This trial does not accept healthy volunteers

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 population

The analyzed population will include adult patients operated on for the most common surgical conditions. Since this will be a multicenter study, the data will include different populations. The analyzed population will be fairly uniform in terms of indications for surgery. The analyzed cases will be diverse in terms of comorbidities, age, and gender.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

500 Participants
are grouped into 2 trial groups
Group A: Laparotomy
Group B: Laparoscopic/robotic

Trial outcomes

Primary outcomes

1

Incisional hernia

Occurrence of postoperative abdominal hernia in the incision line.

Time frame
From the moment of inclusion until one year from the date of surgery.
2

Port-site hernia

Occurrence of port-site hernia after laparoscopy.

Time frame
From the moment of inclusion until one year from the date of surgery.
3

Parastomal hernia

Occurrence of a parastomal hernia after open/laparoscopic stoma formation

Time frame
From the moment of inclusion until one year from the date of surgery.

Secondary outcomes

1

Burst abdomen

Occurrence of burst abdomen after surgery.

Time frame
From the moment of inclusion in the study until 30 days after surgery.
2

Surgical site infection

Occurrence of surgical site infection.

Time frame
From the moment of inclusion in the study until 30 days after surgery or 90 days in the case of mesh use (if the primary procedure was repair of an incarcerated hernia or the mesh was placed to prevent postoperative hernia).

Other outcomes

Sponsors and contacts

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