drugset / Trial / NCT03443141

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

NCT03443141

Phase 3 Unknown 120 enrolled Hospital General Universitario Elche
RandomizedParallel-groupDouble-blindPrevention

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.

Timeline

Start
2018-01-01
Primary completion
2018-03-30
Completion
2018-03-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Vitamin E Other / unclassified

Indications

No indication recorded.