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Evaluation of Long-Term Clinical Acceptability and Satisfaction With the IC-8 Intraocular Lens

NCT03314766 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 64

Last updated 2022-05-13

No results posted yet for this study

Summary

The purpose of this study is to evaluate the long-term clinical acceptability and overall satisfaction with the IC-8 IOL at least 12 months post-IOL implantation.

Conditions

Interventions

DEVICE

IC-8 IOL

Patients previously implanted with an IC-8 IOL contralaterally or bilaterally will be evaluated for their long-term visual functions and overall satisfaction at least 12 months post-implantation

Sponsors & Collaborators

  • AcuFocus, Inc.

    lead INDUSTRY

Principal Investigators

  • Nicholas Tarantino, OD

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-10-20
Primary Completion
2018-11-27
Completion
2018-11-27

Countries

  • Germany
  • Italy
  • Norway
  • Spain

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 NCT03314766 on ClinicalTrials.gov