Examination of the Effect of Skin Antisepsis With Pre-heated Povidone Iodine on Surgical Site Infections: A Quasi-Experimental Study

NACompletedINTERVENTIONAL
Enrollment

124

Participants

Timeline

Start Date

September 28, 2021

Primary Completion Date

December 28, 2021

Study Completion Date

July 28, 2022

Conditions
Surgical Site Infections
Interventions
DIAGNOSTIC_TEST

Follow-up

"The primary outcome of this study was SSI within 30 days of surgery, as defined by the Centers for Disease Control and Prevention. Secondary outcomes were identification of the causative organism, and investigation of clinical factors such as body mass index (BMI), operation time, days of hospitalization, etc. that may be associated with SSI.~All patients were followed up for SSI until discharge from hospital and at the outpatient visits. SSI surveillance data forms were used for the collection of primary and secondary outcome data.~SSI rates and distribution of identified micro-organisms for each group will measured"

Trial Locations (1)

Unknown

Eastern Mediterranean University, Famagusta

All Listed Sponsors
lead

Eastern Mediterranean University

OTHER

NCT04969302 - Examination of the Effect of Skin Antisepsis With Pre-heated Povidone Iodine on Surgical Site Infections: A Quasi-Experimental Study | Biotech Hunter | Biotech Hunter