Efficacy and Safety of ReLEx Smile for Laser Correction of Myopia

University of Aarhus

Status: Completed

Conditions: Myopia

Study type: Observational

Funder types: Other

Identifiers

NCT01481792

AUH-Ophthalmology-2011-01

Details and patient eligibility

About

Evaluation of the safety and efficacy of the Carl Zeiss Meditec VisuMax femtosecond laser for lamellar resection (ReLEx smile) in the reduction of myopia.

Full description

Quality control study of patients treated with ReLEx smile for myopia at the Department of Ophthalmology, Aarhus University Hospital.

The patients will be followed with standard clinical techniques (slit-lamp examination, refraction, topography) during their normal follow-up up to 12 months after treatment.

Enrollment: 125 patients

Sex: All

Ages: 18 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Indication for keratorefractive correction of myopia
• Patient consent to undergo keratorefractive correction of myopia

Exclusion criteria

• Pregnant or lactating women