Purpose: To analyze uveal and capsular biocompatibility 1 year following implantation of a sharp-edged, hydrophilic, collagen-containing posterior chamber intraocular lens (IOL).
Setting: Department of Ophthalmology, University of Vienna Medical School, Vienna, Austria.
Method: In a prospective study, a Collamer CC4204BF IOL was implanted in 30 eyes of patients with senile cataract.