UnknownPhase 3

Corneal Cross-Linking Comparing Variables

United States500 participantsStarted 2014-05

Plain-language summary

The purpose of this study is to evaluate the Safety and Efficacy of Corneal Cross Linking in a Continuous Beam versus Pulsed Treatments across epithelium on and epithelium off surfaces.

Who can participate

Age range12 Years

SexALL

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Inclusion criteria

✓. An increase of ≥ 1.00 D in the steepest keratometry value
✓. An increase of ≥ 1.00 D in astigmatism manifest refraction
✓. A myopic shift (decrease in the spherical equivalent) of ≥ 0.50 D on subjective manifest refraction
✓. Steepening by topography
✓. Thinning of cornea
✓. Shift in the position of thinnest portion of cornea
✓. Change in refraction with increasing myopia
✓. Development of myopic astigmatism

What they're measuring

Visual Acuity

Timeframe: 2 years

Trial details

NCT IDNCT02095730

SponsorCrowd Health Research, LTD

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2016-05

Contact for this trial

Travis A Johnson, Bachelor's

571-234-5678 tjohnson@libertylasereye.com

View on ClinicalTrials.gov More Unstable Corneas trials