CompletedPhase 3

A Prospective Study of Femtosecond Laser Intracorneal Lensectomi

Denmark35 participantsStarted 2011-05

Plain-language summary

The purpose of this study is to compare visual acuity, safety, predictability, corneal biomechanics, dry eyes, and nerve-morphology after all femtosecond laser refractive lenticule extraction. Approximately 30 to 40 patients with moderate to high myopia will randomly (after ocular dominance) receive ReLEx flex in one eye, and ReLEx smile in the other.

Who can participate

Age range25 Years – 45 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * 25 to 45 years, * moderate to high myopia with astigmatism =\< 2 D, * otherwise eye healthy, * CDVA of 0.8 or better (Snellen). Exclusion Criteria: * systemic or ocular disease or previous eye surgery, * thin cornea, * a difference of more than 2 D myopia in the eyes of each subject.

What they're measuring

Visual acuity

Timeframe: up to 6 months

Trial details

NCT IDNCT01673503

SponsorOdense University Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

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