The objective of this study was to evaluate clinical acceptability, delivery characteristics and clinical outcomes in patients implanted with new generation hydrophobic acrylic Intraocular Lens with Preloaded delivery system.
This was a single centre retrospective study.
Total 41 patients were enrolled in the study to get at least 38 patients for evaluation.
All patients were assessed on day1 and 1, 3 and 6 months after surgery.
EYECRYL-SERT showed ‘excellent’ ease of insertion and handling in all 41(100%) patients.
Corrected Distance Visual Acuity (CDVA) improved from 0.74±0.58 logMAR during screening to 0.03±0.04 logMAR 6 months after surgery.
