Evaluation of an Hydrophilic Acrylic Intraocular Lens

Clinical Trial Description

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

Study Design

Related Conditions & MeSH terms

See also
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NCT number	NCT04793789
Study type	Observational
Source	Carl Zeiss Meditec AG
Contact
Status	Completed
Phase
Start date	April 27, 2021
Completion date	January 24, 2022

Evaluation of an Hydrophilic Acrylic Intraocular Lens

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms