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Safety and Efficacy of Intracameral Zimoxin for Prevention of Endophthalmitis After Cataract Surgery

Endophthalmitis Clinical Trial

Official title:
Safety and Efficacy of Intracameral Zimoxin (0.1% Moxifloxacin Solution) for Prevention of Endophthalmitis After Cataract Surgery

Clinical Trial Summary

Intracameral injection of 0.1% moxifloxacin solution after cataract surgery to prevent endophthalmitis

Clinical Trial Description

Subjects will receive either intracameral injection of 0.1% moxifloxacin solution or placebo after cataract surgery. They will be followed for one month to determine if there is a statistically significant difference in the incidence of endophthalmitis. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03244072
Study type Interventional
Source Zion Therapeutics, LLC
Contact Jason Ahee, M.D.
Phone 435-862-9865
Email aheejason@hotmail.com
Status Not yet recruiting
Phase Phase 2/Phase 3
Start date June 1, 2024
Completion date October 2025
View Details
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