Safety and Performance of Hydrophobic and Hydrophilic Intraocular Lenses After Bilateral Cataract Surgery

NCT06192901 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 8

Last updated 2024-01-05

No results posted yet for this study

Summary

Subjects who had a bilateral age-related cataract surgery with the IOLs AT ELANA 841P and AT LISA tri 839MP will be contacted and invited to attend a postoperative visit more than one year after the surgery

Conditions

  • Senile Cataract

Sponsors & Collaborators

  • Carl Zeiss Meditec AG

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-09-18
Primary Completion
2023-09-22
Completion
2023-09-22

Countries

  • El Salvador

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 NCT06192901 on ClinicalTrials.gov