Effect of Vitamin E-containing Dressing on Surgical Site Infection in Colorectal Surgery
Status:
Unknown status
Trial end date:
2018-03-30
Target enrollment:
Participant gender:
Summary
A prospective, randomized study will be performed. Patients are randomized using a 1:1
allocation into 2 groups: patients receiving a vitamin E-containing dressing (group 1) and a
conventional dressing (group 2). The primary outcomes variable will be occurrence of
incisional SSI. Follow-up will be 30 days postoperatively.
Phase:
Phase 3
Details
Lead Sponsor:
Hospital General Universitario Elche
Treatments:
alpha-Tocopherol Tocopherols Tocotrienols Vitamin E Vitamins