Clinical Trials Directory

Trials / Completed

CompletedNCT00673803

Influence of Two Different Preloaded Intraocular Lens (IOLs) on Posterior Capsule Opacification

Influence of Two Sharp-edged Hydrophobic Acrylic Micro-incision-IOLs on Posterior Capsule Opacification. A Randomized, Double-masked Study With Intraindividual Comparison.

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Hospital Hietzing · Academic / Other
Sex
All
Age
55 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Studies showed that a sharp posterior optic edge of an intraocular lens (IOL) inhibits migration of lens epithelial cells in between posterior capsule and optic of the IOL and therefore reduces the rate of posterior capsule opacification (PCO). In present time most IOLs implanted have a sharp posterior optic edge. Due to differences in IOL production different IOLs have different rates of PCO. Progression in cataract surgery technique allow phacoemulsification through micro-incisions. Therefore there is need for IOLs that can be implanted through incisions of about 2.5 mm. This study investigates the effect of two different hydrophobic acrylic IOLs with a sharp posterior optic edge on the rate of PCO after implantation through a micro-incision. The results will be compared intraindividually.

Detailed description

prospective, randomized, bilateral study with intraindividual comparison, implantation of a Polylens Y10 IOL in one eye and implantation of a Polylens Y30 in the contralateral eye. PCO rate will be detected at 1 year and 2 years.

Conditions

Interventions

TypeNameDescription
PROCEDUREcataract surgerycataract surgery with implantation of an IOL

Timeline

Start date
2008-12-01
Primary completion
2009-07-01
Completion
2010-06-01
First posted
2008-05-07
Last updated
2010-08-17

Locations

1 site across 1 country: Austria

Source: ClinicalTrials.gov record NCT00673803. Inclusion in this directory is not an endorsement.