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Fluoroquinolone Antibiotic

Zimoxin for Cataract Surgery Prevention

Phase 2 & 3
Waitlist Available
Research Sponsored by Jason Ahee, M.D.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
visually significant cataracts
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up subjects will undergo eye examinations at one day, one week, and one month post-operatively
Awards & highlights
All Individual Drugs Already Approved
Approved for 10 Other Conditions

Summary

This trial tests if injecting an antibiotic called moxifloxacin into the eye after cataract surgery can prevent infections. Moxifloxacin is commonly used to prevent infections after cataract surgery. It targets patients who have had cataract surgery and aims to stop bacteria from causing infections.

Who is the study for?
This trial is for individuals with visually significant cataracts who are undergoing surgery. It's not suitable for those allergic to fluoroquinolones or cobalamin (B12).
What is being tested?
The study tests the safety and effectiveness of an eye injection called Zimoxin, which contains moxifloxacin, to prevent infection after cataract surgery compared to a placebo.
What are the potential side effects?
Possible side effects may include irritation in the eye, redness, swelling, or other signs of infection due to the moxifloxacin solution.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I have cataracts that affect my vision significantly.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~subjects will undergo eye examinations at one day, one week, and one month post-operatively
This trial's timeline: 3 weeks for screening, Varies for treatment, and subjects will undergo eye examinations at one day, one week, and one month post-operatively for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Endophthalmitis after cataract surgery

Awards & Highlights

All Individual Drugs Already Approved
Therapies where all constituent drugs have already been approved are likely to have better-understood side effect profiles.
Approved for 10 Other Conditions
This treatment demonstrated efficacy for 10 other conditions.

Trial Design

2Treatment groups
Active Control
Placebo Group
Group I: Treatment groupActive Control1 Intervention
Intracameral injection of moxifloxacin solution after cataract surgery
Group II: Placebo groupPlacebo Group1 Intervention
Intracameral injection of placebo after cataract surgery

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for endophthalmitis involve the use of antibiotics that target bacterial replication and infection. Moxifloxacin, for example, inhibits bacterial DNA gyrase and topoisomerase IV, enzymes essential for DNA replication and transcription. By preventing these processes, moxifloxacin effectively stops bacterial growth and proliferation. This mechanism is crucial for endophthalmitis patients as it helps to rapidly reduce the bacterial load in the eye, thereby minimizing damage to ocular tissues and preserving vision.
The Effectiveness of Intracameral Moxifloxacin Endophthalmitis Prophylaxis for Trabeculectomy.

Find a Location

Who is running the clinical trial?

Jason Ahee, M.D.Lead Sponsor

Media Library

Moxifloxacin (Fluoroquinolone Antibiotic) Clinical Trial Eligibility Overview. Trial Name: NCT03244072 — Phase 2 & 3
Endophthalmitis Clinical Trial 2023: Moxifloxacin Highlights & Side Effects. Trial Name: NCT03244072 — Phase 2 & 3
Moxifloxacin (Fluoroquinolone Antibiotic) 2023 Treatment Timeline for Medical Study. Trial Name: NCT03244072 — Phase 2 & 3
Endophthalmitis Research Study Groups: Treatment group, Placebo group
~40000 spots leftby Oct 2025