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Clinical Trials/NCT01605058
NCT01605058
Unknown
Not Applicable

Visual Performance Adn Quality of Vision Evaluation After Implantation of a Trifocal Intraocular Lens

BMI Southend Hospital1 site in 1 country30 target enrollmentJune 2012
ConditionsCataract

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cataract
Sponsor
BMI Southend Hospital
Enrollment
30
Locations
1
Last Updated
13 years ago

Overview

Brief Summary

The purpose of this study is to evaluate the visual performance of a trifocal intraocular lens at distance, near and intermediate viewing, by way of visual acuity measurement, contrast sensitivity.

Patient satisfaction and quality of vision will also be assessed by way of a questionnaire.

Detailed Description

Monocular and Binocular Unaided (UCVA) and Best Corrected Visual Acuity (BCVA) will be measured at 6m in LogMAR units under photopic conditions (85cd/m2). Subjective Refraction will be performed to establish any residual refractive error will for distance, intermediate and near. Defocus Profiles (visual acuity over imposed defocus) are measured for each patient. The patient observes the 6m LogMAR chart through best distance correction, then defocusing is achieved by the addition of pairs of lenses from +2.00D to -4.00D in 0.50D steps.. The LogMAR acuity will be recorded and the data plotted. Contrast Sensitivity will be evaluated monocularly under photopic (85cd/m2) conditions and mesopic (4cd/m2) using the Pelli-Robson Contrast Sensitivity Chart. Near and intermediate performance will be evaluated using the Radner Reading Charts to assess acuity (LogRAD units) and reading speed in photopic conditions 85cd/m2

Registry
clinicaltrials.gov
Start Date
June 2012
End Date
August 2013
Last Updated
13 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
BMI Southend Hospital
Responsible Party
Principal Investigator
Principal Investigator

Elizabeth Agrippa

Optometrist

BMI Southend Hospital

Eligibility Criteria

Inclusion Criteria

  • Age 40-70yrs
  • Bilateral implantation of a trifocal intraocular lens

Exclusion Criteria

  • existing ocular pathology
  • surgical complications
  • corneal astigmatism \> 1.50DC

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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