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Clinical Trial Summary

Describe the efficacy of the use of topical besifloxacin in reducing the conjunctival microbiota as a prophylactic measure in patients scheduled for cataract surgery.


Clinical Trial Description

Randomized double-blind clinical trial. Study carried out in a single center between January and April 2017. 60 eyes were included that were randomly divided in a 1: 1 ratio into two groups. The first group received placebo (hydroxypropylmethylcellulose drops) while the second group received 0.6% besifloxacin drops four times a day for 3 days. All of them had a conjunctival cul-de-sac culture before and after treatment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04542759
Study type Interventional
Source Instituto de Oftalmología Fundación Conde de Valenciana
Contact
Status Completed
Phase Phase 1
Start date January 2017
Completion date April 2017

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