Clinical Trials Directory

Trials / Completed

CompletedNCT03831074

Posterior Capsule Opacification and Optical Quality of Different Hydrophobic Acrylic Intraocular Lenses

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
Sponsor
Medical University of Vienna · Academic / Other
Sex
All
Age
40 Years
Healthy volunteers
Not accepted

Summary

The most frequent long-term complication of cataract surgery remains to be posterior capsule opacification (PCO). During the past decades many new intraocular lenses (IOL) with optimized lens material and design were introduced. We propose a study comparing three acrylic single-piece IOLs with different design and hydrophobic material. All IOLs (Hoya NY-60, HOYA Surgical Optics GmbH; EyeCee One, Nidek Co., Aichi, Japan) are commercially available and are used for routine cataract surgery. In this study a comparison of PCO score of all two IOLs, a comparison of optic quality with wavefront analyses, visual acuity, contrast sensitivity, IOL decentration and tilt, slitlamp examination, fibrosis, glistening intensity (subjectively scored), YAG capsulotomy rate, and safety parameters (IOL related adverse reactions) of the investigated IOLs will be performed. Since PCO develops slowly within years, a long-term follow-up of three years will be necessary. As those IOLs are currently often implanted IOLs, their performance on PCO development and their optical quality is of high interest for the ophthalmologic community.

Conditions

Interventions

TypeNameDescription
DEVICEImplantation of an intraocular lenses: iMics 1 NY-60 & NY-60G

Timeline

Start date
2012-01-27
Primary completion
2015-07-07
Completion
2015-07-07
First posted
2019-02-05
Last updated
2019-02-05

Source: ClinicalTrials.gov record NCT03831074. Inclusion in this directory is not an endorsement.