CompletedPhase 3ACTRN12606000406505

Clinical efficacy of Moxifloxacin in the treatment of Bacterial Keratitis: A Randomised Clinical Trial


Sponsor

Centre for Eye Research Australia

Enrollment

229 participants

Start Date

Oct 9, 2002

Study Type

Interventional

Conditions

Summary

To determine the clinical efficacy and safety of moxifloxacin (1.0%) in patients treated with bacterial keratitis compared with patients treated with ofloxacin (0.3%) or fortified tobramycin (1.33%)/cephazolin (5%).


Eligibility

Sex: Both males and femalesMin Age: 1 Years

Plain Language Summary

Simplified for easier understanding

This study compares moxifloxacin eye drops with standard treatment for bacterial keratitis (a bacterial infection of the cornea). People aged 1 year and older with a diagnosis of bacterial keratitis can join. Participants use the study eye drops and attend follow-up visits so doctors can track healing.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

To determine clinical efficacy and safety for topical moxifloxacin (1.0%) in patients treated with bacterial keratitis. A comparison will be made to patients treated with topical ofloxacin (0.3%) or t

To determine clinical efficacy and safety for topical moxifloxacin (1.0%) in patients treated with bacterial keratitis. A comparison will be made to patients treated with topical ofloxacin (0.3%) or topical fortified tobramycin (1.33%)/cephazolin(5%). After corneal specimens are obtained, the assigned study medication is to be instilled every hour day and night for 48 hours and on the third day every hour by day and every two hours at night. For days four and five one drop every two hours by day and every four hours at night and for days six and seven one drop every four hours. After day seven, the antibiotic is to be tapered to six hourly and stopped when when the ulcer has healed.


Locations(1)

Australia

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ACTRN12606000406505


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