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Clinical Trial Summary

The investigational device is an approved femtosecond laser (FSL) device with an integrated imaging system to perform certain steps of the cataract procedure including arcuate incisions (AI) correcting astigmatism, also referred to as arcuate keratotomy (AK). The FSL will perform anterior capsulotomy and lens fragmentation in individuals suffering from age-related cataract with need of cataract surgery and additionally perform arcuate keratotomy in individuals with more than 1.0 Diopter (dpt) of astigmatism. Cataract surgery will be performed in subjects who have signed an informed consent form. Postoperative examinations will be implemented in accordance with the approved Investigational Plan on subjects and includes: postoperative refraction, visual acuity, slitlamp examination, and corneal topography


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04321226
Study type Interventional
Source Medical University of Vienna
Contact Luca Schwarzenbacher, MD
Phone 0140400
Email luca.schwarzenbacher@meduniwien.ac.at
Status Recruiting
Phase Phase 4
Start date July 10, 2017
Completion date April 1, 2022

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