Parastomal hernia
Conditions
Interventions
Experimental group:In the experimental group (prophylactic mesh group), a non-absorbable 15*20cm artificial mesh was placed by laparoscopic sugarbaker method during MILES operation for rectal cancer.
Control group:No prophylactic mesh was placed in the control group
Sponsors
The First Hospital of China Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: 1. Older than 18 years old 2. Patients who underwent laparoscopic MILES surgery for rectal cancer due to malignancy 3. No history of intestinal surgery 4. Sign the informed consent form in person
Exclusion criteria
Exclusion criteria: 1. Patients who are intolerant to mesh or allergic to mesh 2. Emergency surgery or non-laparoscopic approach 3. Patients with previous abdominal wall hernia or mesh placement at the surgical site 4. Life expectancy less than one year
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Parastomal hernia; | — |
Secondary
| Measure | Time frame |
|---|---|
| The stoma prolapsed;Obstruction of stoma;Mesh infection; | — |
Countries
China
Contacts
Public ContactJianping Zhou
The First Hospital of China Medical University
Outcome results
None listed