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LFA-1/ICAM-1 Antagonist
Lifitegrast for Dry Eye Syndrome
Phase 4
Waitlist Available
Led By Frank A Bucci, Jr., MD
Research Sponsored by Bucci Laser Vision Institute
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Positive for MMP-9 bilaterally as assessed by the Inflammadry assay
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 weeks
Awards & highlights
Study Summary
This trial will test whether Xiidra can reduce inflammation of the eye surface in both pre- and post-operative cataract patients.
Eligible Conditions
- Dry Eye Syndrome
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 12 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Compare the conversion rates of bilateral positive MMP-9 to negative in pre-cataract and post-cataract patients receiving treatment with Xiidra versus no Xiidra
Trial Design
2Treatment groups
Active Control
Group I: ControlActive Control1 Intervention
No treatment
Group II: LifitegrastActive Control1 Intervention
One drop of Lifitegrast Ophthalmic Solution 5% will be instilled into each eye twice daily (approximately 12 hours apart) using a single-use conainer.
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Who is running the clinical trial?
Bucci Laser Vision InstituteLead Sponsor
6 Previous Clinical Trials
264 Total Patients Enrolled
Frank A Bucci, Jr., MDPrincipal InvestigatorBucci Laser Vision
5 Previous Clinical Trials
513 Total Patients Enrolled
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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