Evaluation of Visual Outcomes in Patients With Complex Corneas Implanted With the IC-8 IOL

NCT05377515 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 21

Last updated 2023-05-10

No results posted yet for this study

Summary

The purpose of this study is to evaluate visual outcomes in patients with complex corneas who have been previously implanted with the IC-8 IOL after cataract removal.

Conditions

  • Cataract
  • Presbyopia
  • Irregular; Contour of Cornea

Sponsors & Collaborators

  • AcuFocus, Inc.

    lead INDUSTRY

Principal Investigators

  • Magda Michna, Ph.D. · AcuFocus, Inc.

Eligibility

Min Age
22 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-02-10
Primary Completion
2022-12-30
Completion
2022-12-30

Countries

  • Singapore

Study Locations

More Related Trials

Entities

Diseases

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 NCT05377515 on ClinicalTrials.gov