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Integrin Antagonist
nanomicellular cyclosporine 0.09% for Dry Eye Syndrome
Phase 4
Recruiting
Research Sponsored by Toyos Clinic
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 90 days
Awards & highlights
Study Summary
This trial will compare the effectiveness of two different eye drops in reducing corneal staining before cataract or LASIK surgery.
Eligible Conditions
- Dry Eye Syndrome
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 90 days
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~90 days
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
change in central corneal staining
Secondary outcome measures
change in OSDI questionnaire with additional questions of dysgeusia, blurriness and sensation of burning
change in Schirmers testing
change in corneal topography
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Nanomicellular Cyclosporine 0.09 prior to surgeryExperimental Treatment1 Intervention
50 subjects receive nanomicellular cyclosporien 0.09% prior to elective ophthalmic surgery
Group II: Lifitegrast 5.0%Active Control1 Intervention
50 subjects receive liftigrast 5.0% prior to elective ophthalmic surgery
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Who is running the clinical trial?
Toyos ClinicLead Sponsor
8 Previous Clinical Trials
160 Total Patients Enrolled
Sun Pharmaceutical Industries LimitedIndustry Sponsor
64 Previous Clinical Trials
13,411 Total Patients Enrolled
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