Visual Performance With a Trifocal Intraocular Lens
Recruitment status was: Not yet recruiting
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.
|Study Design:||Observational Model: Cohort
Time Perspective: Retrospective
|Official Title:||Visual Performance Adn Quality of Vision Evaluation After Implantation of a Trifocal Intraocular Lens|
|Study Start Date:||June 2012|
|Estimated Study Completion Date:||August 2013|
|Estimated Primary Completion Date:||July 2013 (Final data collection date for primary outcome measure)|
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
Please refer to this study by its ClinicalTrials.gov identifier: NCT01605058
|BMI Southend Hospital|
|Westclifff-on-Sea, Essex, United Kingdom, SS0 9AG|
|Principal Investigator:||Elizabeth M Agrippa, BSc||BMI Southend|