A Prospective Observational Case Series of a Four-ring-haptic Acrylic One-piece IOL

NCT01244373 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 9

Last updated 2010-11-19

No results posted yet for this study

Summary

To describe biocompatibility, postoperative results and complications after implantation of the Corneal Quatrix Evolutive (Corneal, Croma, Austria) intraocular lens, a hydrophilic acrylic intraocular lens (IOL) with 4-haptic design and 360° sharp optic edge.

Conditions

  • Cataract

Sponsors & Collaborators

  • Department of ophthalmology, General Hospital Linz

    collaborator UNKNOWN
  • General Hospital Linz

    lead OTHER

Eligibility

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

Timeline & Regulatory

Start
2008-05-31
Primary Completion
2009-08-31
Completion
2009-08-31

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 NCT01244373 on ClinicalTrials.gov