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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. The FSL will perform anterior capsulotomy and lens fragmentation in individuals suffering from age-related cataract with need of cataract surgery.

Cataract surgery will be performed in subjects who have signed an informed consent form. Macula thickness will be measured with Spectralis OCT on screening date.

Postoperative examinations will be implemented in accordance with the approved investigational plan on subjects and includes: visual acuity, slitlamp examination, retinal oct imaging and quantitative autofluorescence.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03465124
Study type Interventional
Source Medical University of Vienna
Contact
Status Active, not recruiting
Phase N/A
Start date March 26, 2018
Completion date April 6, 2019

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