Effect of Vitamin E-containing Dressing on Surgical Site Infection in Colorectal Surgery

Category Primary study
Registry of Trialsclinicaltrials.gov
Year 2018
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.
Epistemonikos ID: 9618d53bf825598ee42b06b82e522bdc9967628f
First added on: May 21, 2024