Umbilical Hernia
Conditions
Keywords
umbilical, hernia, mesh
Brief summary
The purpose of the present study is to investigate whether or not the use of mesh is indicated in the repair of all size umbilical hernias as to reduce the rate of recurrence. This method is regularly used in umbilical hernia reconstruction although most surgeons repair small hernias using suture repair (fascia adaptation). Especially risk factors for hernia recurrence such as hernia size and BMI \> 30 kg/m2 need to be evaluated and correlated to the method of hernia repair.
Detailed description
Purpose The purpose of the present study is to investigate whether or not the use of mesh is indicated in the repair of all size umbilical hernias as to reduce the rate of recurrence. This method is regularly used in umbilical hernia reconstruction although most surgeons repair small hernias using suture repair (fascia adaptation). Especially risk factors for hernia recurrence such as hernia size and BMI \> 30 kg/m2 need to be evaluated and correlated to the method of hernia repair. Study design Randomised controlled, double blinded, multi-centre trial. 300 consecutive patients with an umbilical hernia will be included in the study. Patients will be randomised in one of two groups of 150 patients each. Group 1 will include patients that will undergo primary (suture) repair; group 2 umbilical hernias will be repaired using a pre-peritoneal, flat polypropylene mesh in a tension free fashion. Stratification will be utilized for the size of the hernia (1-2 cm or ≥2-4 cm) and the participating centre. Patients will visit the outpatient clinic after 2-3 weeks and after 3, 12 and 24 months. The cumulative hernia recurrence rate during the 2-years follow-up period will be the primary outcome of the study. Complications, pain and QOL are secondary endpoints. Statistical analysis All analyses will be performed according to the intention to treat principle and as specified in the protocol. Financial support None.
Interventions
primary suture closure of hernia
mesh enforced closure of hernia
Sponsors
Study design
Intervention model description
Suture versus mesh repair in umbilical hernia patients
Eligibility
Inclusion criteria
* Primary umbilical hernia * Signed Informed consent
Exclusion criteria
* Umbilical hernia ≥ 4 cm diameter * Recurrence * Midline laparotomy * Ascites/Cirrhosis * ASA score IV or above * Incarcerated hernia/emergency procedures
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| hernia recurrence rate | 24 months |
Secondary
| Measure | Time frame |
|---|---|
| Post-operative morbidity and complications | 3 months |
Countries
Germany, Italy, Netherlands