drugset / Trial / NCT06710977

To Compare the Safety and Efficacy of Intracameral Levofloxacin and Intracameral Cefazolin in Reducing Rates of Endophthalmitis Following Cataract Surgery.

NCT06710977

Phase 0 Completed 50 enrolled Tan Tock Seng Hospital
RandomizedParallel-groupQuadruple-blindSupportive care

Summary

Patients with senile cataracts undergoing phacoemulsification were assigned to receive intracameral levofloxacin (0.1ml/0.5mg) or intracameral cefazolin (0.1ml/1mg). The primary endpoint was the occurrence of endophthalmitis during the 3 month follow-up period. Secondary endpoints included best-corrected visual acuity (BVCA), the presence of anterior chamber (AC) inflammation with grading of AC cells and presence of flare, along with intraocular pressure (IOP), corneal cell thickness (CCT), central foveal thickness (CFT) and cell density.

Timeline

Start
2022-01-01
Primary completion
2024-09-01
Completion
2024-09-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Cefazolin Small molecule 0.1 ml Other
Subject Cefazolin Small molecule 1 mg Other
Subject Levofloxacin Small molecule 0.1 ml Other
Subject Levofloxacin Small molecule 0.5 mg Other

Indications