Air Optix contact lens for Corneal Abrasions

Phase-Based Progress Estimates
1
Effectiveness
1
Safety
Corneal AbrasionsAir Optix contact lens - Device
Eligibility
18+
All Sexes
What conditions do you have?
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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

1 of 3

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

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: Device
Usual 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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