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Long-term Follow-up of Prophylactic Mesh Reinforcement After Emergency Laparotomy.

J

José A. Pereira

Status

Completed

Conditions

Prevention of Incisional Hernia in Emergency Surgery

Treatments

Procedure: Prophylactic mesh use

Study type

Observational

Funder types

Other

Identifiers

NCT04578561
20198240I

Details and patient eligibility

About

Observational Study analyzing the long-term results of prophylactic mesh used for preventing incisional hernia after emergency midline laparotomies.

Full description

Background. Prevention of incisional hernias with a prophylactic mesh in emergency surgery is controversial. The present study aimed to analyze the long-term results of prophylactic mesh used for preventing incisional hernia after emergency midline laparotomies.

Methods. This study was a retrospective analysis of patients who underwent an emergency midline laparotomy between January 2009 and July 2010 with a follow-up period of longer than 2 years. Long-term outcomes and risk factors for the development of incisional hernias between patients who received a prophylactic reinforcement mesh (Group M) and suture (Group S) were compared.

Enrollment

187 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients undergoing emergency midline laparotomy

Exclusion criteria

  • Those with need of concomitant hernia repair.
  • Those who received incisions outside the midline.
  • Those with delayed abdominal closure.
  • Those who died in the immediate postoperative period.
  • Those without a minimum 2 years of follow-up.

Trial design

187 participants in 2 patient groups

Prophylactic mesh
Description:
Patients who received a prophylactic mesh after emergency surgery due to high risk of incisional hernia.
Treatment:
Procedure: Prophylactic mesh use
Suture
Description:
Patients who's laparotomies closure was using only suture without any abdominal wall reinforcement

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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