Acrylate Intraocular Lenses in Cataract Surgery of Uveitis Patients

Comparison of Two Different Acrylate Intraocular Lenses in Cataract Surgery in Patients With Non-infectious Uveitis

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT00403832

Enrollment

Registered

2006-11-27

Start date

2005-08-31

Completion date

2007-02-28

Last updated

2010-07-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cataract, Uveitis

Brief summary

Cataract is a common complication in uveitis patients. Cataract operations with intraocular lens implantation are difficult in these patients because of complication due to the biocompatibility of the intraocular lens. In this study, uveal and capsular biocompatibility of two widely used acrylate intraocular lenses are compared.

Interventions

DEVICEintraocular lenses: Two foldable, acrylic, sharp edged IOLs: AcrySof™ (AcrySof SA60AT, Alcon), and Akreos adapt™ (Bausch & Lomb)

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* non infectious uveitis * no active inflammation * significant visual disturbance related to lens opacification

Exclusion criteria

* vitreous opacification * ocular hypertension/glaucoma

Design outcomes

Primary

Measure	Time frame
visual acuity	—
cell deposits on anterior IOL surface	—
posterior capsular opacification	—

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026