Study Summary
This trial is testing if a bandage contact lens helps heal a corneal abrasion better than the usual treatment.
Eligible Conditions
- Corneal Abrasions
Treatment Effectiveness
Effectiveness Progress
Study Objectives
2 Primary · 0 Secondary · Reporting Duration: Baseline, approx. 12-24 hours, approx. 36-48 hours, approx. 1 day, 3 days, and/or 5 days post-discharge
Day 5
Change in Pain Score
Change in pain score
Trial Safety
Safety Progress
Trial Design
2 Treatment Groups
Usual Care Group
1 of 2
Bandage Contact Lens (BCL) group
1 of 2
Active Control
Experimental Treatment
1 Total Participants · 2 Treatment Groups
Primary Treatment: Air Optix contact lens · No Placebo Group · N/A
Bandage Contact Lens (BCL) group
Device
Experimental Group · 1 Intervention: Air Optix contact lens · Intervention Types: DeviceUsual Care GroupNoIntervention Group · 1 Intervention: Usual Care Group · Intervention Types:
Trial Logistics
Trial Timeline
Screening: ~3 weeks
Treatment: Varies
Reporting: baseline, approx. 12-24 hours, approx. 36-48 hours, approx. 1 day, 3 days, and/or 5 days post-discharge
Who is running the clinical trial?
Mayo ClinicLead Sponsor
2,922 Previous Clinical Trials
3,517,152 Total Patients Enrolled
Robert HydePrincipal InvestigatorMayo Clinic
Eligibility Criteria
Age 18+ · All Participants · 1 Total Inclusion Criteria
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Conditions
Cancer Related
Treatments