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Comparison Between a Toric Monofocal and Multifocal Intraocular Lens

NCT04907318 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 60

Last updated 2021-06-02

No results posted yet for this study

Summary

The primary objective of the study is to observe the rotational stability of the implant 30 minutes, one day, 6 weeks, 6 months and 12 months after the implant surgery. In addition, the refraction will be measured as it is directly affected in the event of postoperative rotation. The correlation between postoperative rotation and the following parameters will be determined: PEXS, white-to-white, age, axial length, anterior chamber depth. Visual acuities with and without correction and the best refraction to assess the benefit of the implants will also be investigated.

Conditions

  • Cataract

Interventions

DEVICE

Cataract surgery

Sponsors & Collaborators

  • Beaver-Visitec International, Inc.

    lead INDUSTRY

Principal Investigators

  • Kristof Vandekerckhove, MD · Vista Alpina Eye Cente, Visp, Switzerland, 3930

Eligibility

Min Age
18 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-01-01
Primary Completion
2016-06-01
Completion
2016-07-01

Countries

  • Switzerland

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 NCT04907318 on ClinicalTrials.gov