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Treatment of Residual Myopic Refraction After 6 Months on Pseudophakic Patients Using Relex-Smile — Relex-Smile  

Myopia Clinical Trial

Official title:
Treatment of Residual Myopic Refraction After 6 Months on Pseudophakic Patients Using Relex-Smile

Clinical Trial Summary

The aim of this study is to assess visual and refractive outcomes after laser vision correction (LVC) - ReLex Smile to correct residual myopic refraction after 6 months of pseudophakic (IOL) implantation. Before SMILE YAG-Laser capsulotomy should be performed on all patients, regardless of posterior capsule ossification, in pseudophakic patients with residual refraction. When the YAG Laser is applied after the SMILE, there will be a diopter change.

Clinical Trial Description

The residual myopic refraction after 6 month on pseudophakic patients using Relex-Smile surgery using VisuMax Femtosecond Laser.The residual myopic refractive power is between -0.75D till -5.50D.The optical zone(lenticule diameter) and cap diameter were 6.5 and 7.5 mm respectively.After dissection of both anterior and posterior planes, the lenticule was extracted through 120 degree superior 3.5mm incision and marked with a sterile marker(Viscot-Medster) ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04693663
Study type Interventional
Source Eye Hospital Pristina Kosovo
Contact
Status Enrolling by invitation
Phase N/A
Start date June 1, 2017
Completion date June 1, 2024
View Details
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