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Observation of Rotation of an Intraocular Lens

NCT02208232 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2014-08-05

No results posted yet for this study

Summary

The purpose of this study is to assess the axial IOL rotation after surgery with an MC 6125 AS IOL.

At the end of surgery the orientation of the IOL is documented with a short video clip via the operating microscope unit. Follow-up examinations are performed 1 hour, 1 week and 6 months after surgery. Rotational stability of the IOL is assessed using retroillumination images with a method to avoid bias from cyclorotation or head tilt.

Conditions

  • Cataract

Interventions

PROCEDURE

cataract surgery

cataract surgery with implantation of intraocular lens

Sponsors & Collaborators

  • Medical University of Vienna

    lead OTHER

Eligibility

Min Age
40 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-06-30
Primary Completion
2012-12-31
Completion
2012-12-31

Countries

  • Austria

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 NCT02208232 on ClinicalTrials.gov