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Clinical Trials/NCT01250054
NCT01250054
Completed
Not Applicable

Comparison of Two Multifocal Contact Lenses

CIBA VISION0 sites17 target enrollmentOctober 2010
ConditionsPresbyopia

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Presbyopia
Sponsor
CIBA VISION
Enrollment
17
Primary Endpoint
Overall Vision
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

The purpose of this study is to compare two multifocal contact lenses in presbyopic wearers.

Registry
clinicaltrials.gov
Start Date
October 2010
End Date
October 2010
Last Updated
13 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
CIBA VISION
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • At least 35 years of age.
  • Sign written Informed Consent
  • Spectacle add of +0.50 to +2.50D.
  • Best corrected visual acuity of at least 20.30 in both eyes.
  • Currently wearing soft contact lenses at least 5 days per week.
  • Other protocol-defined inclusion criteria may apply.

Exclusion Criteria

  • Eye injury or surgery within twelve weeks of enrollment.
  • Currently enrolled in any clinical trial.
  • Astigmatism \> 1.00D.
  • Strabismus/amblyopia.
  • Other protocol-defined exclusion criteria may apply.

Outcomes

Primary Outcomes

Overall Vision

Time Frame: One week of wear

Overall vision, as interpreted by the participant and recorded by the investigator as a single, retrospective evaluation of one week's wear time. Overall vision was measured on a 10-point scale, with 1 being worst and 10 being best.

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