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A Multi Focal Visual Outcome Study Using Different Near Additions

NCT00960700 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 52

Last updated 2013-02-08

No results posted yet for this study

Summary

A multi-centre non-randomized clinical investigation to assess multifocal visual outcomes using different near additions, for the treatment of aphakia after cataract removal.

Conditions

  • Cataract
  • Aphakia

Interventions

DEVICE

Visual Acuity

Assessment of visual acuity

DEVICE

Contrast sensitivity

Assessment of contrast sensitivity

DEVICE

Reading Speed

Assessment of reading speed

PROCEDURE

Eye Health

Examination of eye health through use of a slitlamp/ photography. Assessment of Intraocular Pressure.

Sponsors & Collaborators

  • Rayner Intraocular Lenses Limited

    lead INDUSTRY

Principal Investigators

  • Gerd U Auffarth, Prof.

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-09-30
Primary Completion
2011-08-31
Completion
2011-08-31

Countries

  • Germany
  • Lithuania

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 NCT00960700 on ClinicalTrials.gov