K43 R52 K40.91 K43.98
Conditions
Interventions
Group 1: 2 weeks carrying of an Abdominal binder following laparocopic incisional hernia repair (IPOM technique) (Intraperitoneal onlay mesh)
Group 2: No carrying of an Abdominal binder following inci
Sponsors
Helios Forschungsförderung der Helios Kliniken
Eligibility
Sex/Gender
All
Age
18 Years to 100 Years
Inclusion criteria
Inclusion criteria: Patients who have an incisional hernia Surgical treatment using laparoscopic IPOM technology Cognitive ability to give informed consent
Exclusion criteria
Exclusion criteria: Known HIV infection Refusal to participate in the study on the part of the patient Pregnancy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain after 1.,2. and 14. postoperative day following incisional hernia repair in IPOM technique | — |
Secondary
| Measure | Time frame |
|---|---|
| Seromas, wound infection, relapse on 1st, 2nd and 14th postoperative day Restriction of mobility according to VAS on the 1st, 2nd and 14th postoperative day General well-being according to VAS on the 1st, 2nd and 14th postoperative day Postoperative complications according to the Clavien-Dindo classification and compliance with (NOT) bandaging on the 14th postoperative day Quality of life after one year according to SF36 questionnaire One year recurrence rate | — |
Countries
Germany
Contacts
Public ContactChristoph Paasch
Helios Klinikum Berlin-Buch
Outcome results
None listed