Evaluation of a Trifocal Lens

Status Completed

Clinical Trial Summary

Evaluation of the clinical safety and effectiveness of hydrophilic acrylic intraocular lens

Clinical Trial Description

To show safety and the effectiveness in regard to the monocular corrected distance visual acuity (CDVA), the distance-corrected intermediate visual acuity (DCIVA) and the distance-corrected near visual acuity (DCNVA) at 12-24 month postoperative. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04545671
Study type	Observational
Source	Carl Zeiss Meditec AG
Contact
Status	Completed
Phase
Start date	November 1, 2020
Completion date	March 16, 2022

View Details

See also
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