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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 belowSelect...
I have cataracts that affect my vision significantly.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ subjects will undergo eye examinations at one day, one week, and one month post-operatively
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~subjects will undergo eye examinations at one day, one week, and one month post-operatively
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.
The Effectiveness of Intracameral Moxifloxacin Endophthalmitis Prophylaxis for Trabeculectomy.
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Who is running the clinical trial?
Jason Ahee, M.D.Lead Sponsor
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have cataracts that affect my vision significantly.You are allergic to fluoroquinolones, a type of medication.
Awards:
This trial has 2 awards, including:- 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.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Research Study Groups:
This trial has the following groups:- Group 1: Treatment group
- Group 2: Placebo group
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