The effect of povidone-iodine 10% plus levofloxacin 0.5% before cataract surgery: a randomized clinical trial
- PMID: 40102985
- PMCID: PMC11921663
- DOI: 10.1186/s13104-025-07116-3
The effect of povidone-iodine 10% plus levofloxacin 0.5% before cataract surgery: a randomized clinical trial
Abstract
This study was designed to assess the efficacy of using povidone-iodine (PVI) 10% and levofloxacin 0.5% about one hour before cataract surgery in minimizing aqueous contamination compared with using PVI 10%. The intervention group received three drops of mixed povidone-iodine and levofloxacin (PVI/Levofloxacin) solution one hour before surgery. After making the corneal incision in cataract surgery, 0.1 cc aqueous humor sample was taken and sent for culture. We compared the intervention group and control group using t-test and chi-square test in SPSS 25(Chicago IL, USA). 147 eyes of 147 patients were analyzed. The intervention and control groups consisted of 72 and 75 patients, respectively. The Control group showed significantly more positive cultures (16 cultures: 22.2%). the intervention group had four positive cultures (5.3%). (P-value = 0.005). Topical levofloxacin 0.5% and povidone-iodine 10% mixture showed promising results in reducing the number of bacteria in the aqueous humor.
Keywords: Endophthalmitis; Levofloxacin; Povidone-iodine.
© 2025. The Author(s).
Conflict of interest statement
Declarations. Ethics approval and consent to participate: All methods and experimental protocols were under the tenets of the Declaration of Helsinki and approved by the ethics committee of Shiraz University of Medical Sciences and the Iranian Registry of Clinical Trials (IR.SUMS.MED.REC.1398.610 and IRCT20191023045211N1). Consent to participate was obtained from the patients. Consent for publication: Not applicable. Informed consent: All participants were informed about the interventions, and written informed consents were obtained. Trial registration: This study was a randomized clinical trial that approved by Iranian Registry of Clinical Trials (IRCT20191023045211N1) on 30th March 2023. Source of support: This study was supported by Shiraz University of Medical Sciences and the grant number is 18,707. Competing interests: The authors declare no competing interests.
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