A prospective randomised trial comparing two different skin closure techniques following ileostomy closure.
Recruiting
- Conditions
- Colorectal diseases with the presence of an Ileostomy
- Registration Number
- DRKS00000073
- Lead Sponsor
- niversitätsmedizin Mannheim, Chirurgische Kliniks
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
1) Patients with a planned ileostomy closure
2) Patient compliance
3) Informed consent
Exclusion Criteria
1) Lack of informed consent
2) Participation in other clinical trials
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Rate of wound infection <br>Definition of wound infection: Inflammation of the skin, sectretion of pus or unclear fluid, opening of the wound, antibiotic therapy<br>This will be examined on the 3 ± 1 postoperative day, at discharge, on 30 ± 2 days after the operation
- Secondary Outcome Measures
Name Time Method Cosmetic result: 1 month and 6 months after the operation the cosmetic outcome of the wound will be examined in both groups. The cosmetic result will be examined based on two cosmetic scales: -Body Image Questionnaire-, and the patient scale of the -Patient and Observer Scar Assessment Scale-. <br><br>In addition the lenght of skin closure in minutes, the lenght of the operation in minutes, the postoperative hospital stay in days and the effects of age, gender, nicotin and alcohol consumption, Diabetes, Cortison, BMI, Albumin i.S on the rate of wound infection will be assessed.