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Circular pOlyethylene Drape in preVention of Surgical Site infEction: A Randomized Controlled Trial — COVER  

Surgical Wound Infection Clinical Trial

Official title:
Randomized Controlled Trial to Evaluate the Effectiveness and Efficacy of a Sterile Circular Polyethylene Drape Compared to Conventional Surgical Dressing in Prevention of Surgical Site Infection

Clinical Trial Summary

This study is to evaluate the effectiveness of the plastic ring wound retractor to reduce the rate of surgical site infection in patients who undergo open abdomen surgery for gastrointestinal tract.

Clinical Trial Description

Participants who are determined to undergo open abdomen surgery will be screening for the eligibility first. If eligible and agreed to participate, each participant will be assigned to either the experimental group or control group based on the electronic randomization. The experimental group will use the plastic ring wound retractor, while the control group will use a conventional surgical pad for wound protection method. Each participant will be blind to the randomization result because he/she will be under general anesthesia. Once the surgery is finished, the patient will be assessed on the surgical wound at postoperative day 1, 7, 14, 30. Two groups will be compared for the surgical wound infection rate. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03170843
Study type Interventional
Source Saint Vincent's Hospital, Korea
Contact
Status Completed
Phase N/A
Start date July 12, 2017
Completion date September 30, 2022
View Details
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