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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) at 12-24 month postoperative. ;


Study Design


Related Conditions & MeSH terms


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

See also
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