87
Participants
Start Date
October 31, 2023
Primary Completion Date
October 31, 2025
Study Completion Date
October 31, 2025
AT ELANA
The device is CE-approved. The device is a posterior chamber multifocal intraocular lens (IOL) indicated for aphakia after surgical extraction of the cataractous natural lens. The device is also indicated for non-cataractous, presbyopic patients (PRELEX) who seek greater independence from glasses for intermediate and/or near distances. It is an aspheric (aberration-neutral) IOL made of hydrophobic acrylic material, coated with heparin with modified C-loop haptics.
PVK Precise Vision GmbH, Rheine
Universitätsklinikum Heidelberg, Heidelberg
Ofatlivist Alicante, Alicante
Lead Sponsor
Carl Zeiss Meditec AG
INDUSTRY