Evaluation of Seelens AF, an Aspheric Intra-ocular Lens

Status Withdrawn

Clinical Trial Summary

Senile cataract is managed by cataract extraction and intra-ocular lens (IOL) implantation. The purpose of this study is to evaluate the safety and efficacy of the SeeLens AF, an acrylic hydrophilic aspheric IOL. This lens was designed to reduce vision aberrations and secondary cataract formation rate. Preoperative evaluation: Best corrected visual acuity, refraction, comprehensive slit lamp examination and biometry. Surgical procedure: Cataract surgery using a clear corneal incision (1.8mm to2.4mm), phacoemulsification and implantation of the SeeLens AF to the capsular bag. IOL implantation parameters will be evaluated by the surgeon. Postoperative follow up: Best corrected visual acuity, uncorrected visual acuity, refraction and comprehensive slit lamp examinations up to 3 months after surgery.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Cataract

Clinical Trial Details

NCT number	NCT00825747
Study type	Interventional
Source	Hanita Lenses
Contact
Status	Withdrawn
Phase	N/A
Start date	January 2009
Completion date	January 2010

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