Cornea Ectasia Excimer Laser Treatment

Status Completed

Clinical Trial Summary

To evaluate efficacy, safety, objective and subjective quality of vision after treatment of cornea ectasia with transepithelial topographic guided laser simultaneous Central Corneal Remodeling (CCR) and Cross-linking (CXL).

Clinical Trial Description

Background To evaluate efficacy, safety, objective and subjective quality of vision after treatment of cornea ectasia performed with transepithelial topographic guided laser simultaneous Central Corneal Remodeling (CCR) and Cross-linking (CXL).

Methods In this retrospective study 8 eyes of 8 patients (mean age 31.50±14.73 years) affected by cornea ectasia underwent simultaneous CCR and CXL. Preoperative and 6 month postoperative uncorrected distance visual acuity (UDVC) and distance corrected visual acuity (DCVA) were measured using the Efficacy and Safety index. Objective and subjective quality of vision were evaluated preoperatively and 6 months postoperatively using corneal morphological irregularity index (CMI), National Eye Institute Visual Function NEI-VFQ25 and NEI-VFQ39 questionnaires. ;

Study Design

Related Conditions & MeSH terms

Corneal Ectasia

Clinical Trial Details

NCT number	NCT04405882
Study type	Observational
Source	Bambino Gesù Hospital and Research Institute
Contact
Status	Completed
Phase
Start date	October 1, 2019
Completion date	April 30, 2020

View Details

See also
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