drugset / Trial / NCT03443141
Effect of Vitamin E-containing Dressing on Surgical Site Infection in Colorectal Surgery
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Vitamin E | Other / unclassified | — | — |
Indications
No indication recorded.