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Clinical Trial Summary

The purpose of the present study is to elucidate the qualitative and quantitative variation of ocular flora after treatment with eyedrops containing 0.6% povidone-iodine in the eye of patients undergoing routine cataract surgery.


Clinical Trial Description

Two conjunctival swabs will be executed at 3 days before and at the day of routine cataract surgery in each eye of patients undergoing routine cataract surgery. After the collection of the first conjunctival swab a three-days treatment with eyedrops containing 0.6% povidone-iodine in the eye undergoing routine cataract surgery will be performed. Bacterial isolates will be identified by using standard microbiological protocols and total bacterial load will be determined at the two different time points. In vitro susceptibility testing to determine methicillin resistance in isolated Staphylococcus species will be performed. Controlateral eye of each patient will be used as control. Descriptive statistics will be calculated. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03958292
Study type Interventional
Source Ospedale Sacra Famiglia - Fatebenefratelli Erba
Contact
Status Completed
Phase N/A
Start date January 8, 2018
Completion date March 30, 2019