Inguinal hernia Digestive System Inguinal hernia
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Adult (aged >16 years) native patients 2. Presenting at one of the participating hospitals between October 2018 and March 2020 3. Suffering from reducible primary or recurrent inguinal hernia, either uni- or bilateral
Exclusion criteria
Exclusion criteria: 1. History of laparotomy or retroperitoneal surgery 2. Strangulated or irreductible inguinal hernia 3. Inguinoscrotal hernia 4. Non-inguinal hernia 5. Participant who refused consent to study 6. Participant deemed unfit to undergo general anesthesia
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Operating time (from first skin incision to closure) measured using medical notes (anesthesia sheet) at the end of surgery | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Conversion to open surgery during laparoscopic procedure, measured using medical notes (desaturation, major bleeding, camera failure, difficult dissection, very low blood pressure) during surgery 2. Incidence of seroma measured by physical examination on day 1 to day 90 postoperative 3. Incidence of hematoma measured by physical examination on day 1 to day 30 postoperative 4. Reoperation measured using medical notes (infection, reject of mesh, major bleeding, recurrence, bowel obstruction) on day 1 to month 30 postoperative relative to the primary operation 5. Infection measured using physical examination, temperature over 38°C, blood tests, on day 1 to month 30 postoperative relative to the primary operation 6. Recurrence measured using physical examination on day 1 to month 30 postoperative | — |
Countries
Cameroon