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ACTIVE NOT RECRUITING
NCT02921009
NA

McNeel Eye Center Corneal Crosslinking Study

Sponsor: McNeel Eye Center

View on ClinicalTrials.gov

Summary

This study will investigate the effectiveness in treating keratoconus, pellucid marginal degeneration and post LASIK iatrogenic ectasia utilizing fluence rates and treatment times of Corneal Cross Linking other than the original FDA approved protocol of 3mw/cm2.

Official title: Study of Effectiveness and Safety of Transepithelial Collagen Cross-linking at Varying Fluence Levels.

Key Details

Gender

All

Age Range

15 Years - 50 Years

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2016-09-01

Completion Date

2025-12-31

Last Updated

2025-04-06

Healthy Volunteers

Yes

Conditions

Interventions

DEVICE

Crosslinking using UV light of two different fluence rates

The treatment of keratoconus involves the application of riboflavin followed by Ultraviolet light of differing intensities. This study will determine the effectiveness of a greater UV light fluence at a shorter treatment time than is currently utilized.

Locations (1)

McNeel Eye Center

Boise, Idaho, United States