Safety and Effectiveness of an Hydrophilic Acrylic Intraocular Lens

NCT04789538 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 328

Last updated 2022-05-10

No results posted yet for this study

Summary

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

Conditions

  • Cataract Senile

Interventions

OTHER

monofocal lens

not applicable as patients are already implanted with the monofocal intraocular lens

Sponsors & Collaborators

  • Carl Zeiss Meditec AG

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-08-31
Primary Completion
2022-04-01
Completion
2022-04-01

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04789538 on ClinicalTrials.gov