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Contact Lens Optics and Visual Performance

Contact Lens Optics and Visual Performance

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05308069
Enrollment
24
Registered
2022-04-01
Start date
2022-06-13
Completion date
2022-07-27
Last updated
2022-08-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Myopia

Brief summary

This study will evaluate changes in visual performance at different pupil sizes between a single vision soft contact lens and multifocal soft contact lens, and compare refractive error measured between these two lenses with an autorefractor and an aberrometer

Interventions

Subjects will wear a single vision soft contact lens only during the study visit

Subjects will wear a multifocal soft contact lens only during the study visit

Sponsors

David A Berntsen, OD PhD
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 39 Years
Healthy volunteers
No

Inclusion criteria

* Able to read and understand the informed consent document * 18 to 39 years of age (inclusive) * Best corrected visual acuity of 20/25 or better in the right eye * Refractive error from -1.00D to -8.00D with astigmatism less than or equal to -1.00D in the right eye (corneal plane)

Exclusion criteria

* Any ocular or systemic conditions affecting vision, refraction, or the ability to wear a soft contact lens * History of ocular trauma or surgery causing abnormal or distorted vision * Current Rigid Gas Permeable (RGP) contact lens wearers * Pregnant and/or lactating females, by self-report

Design outcomes

Primary

MeasureTime frameDescription
Visual performanceThrough completion of study visit, an average of 3 hoursLow contrast visual performance will be measured at different pupil sizes for each subject while wearing each of the two lenses

Secondary

MeasureTime frameDescription
Refractive errorThrough completion of study visit, an average of 3 hoursRefractive error will be measured with an autorefractor and an aberrometer with subjects wearing each of the two lenses

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026