Skip to content

Improving Glare and Visual Comfort for Patients With Visual Impairment

Managing Visual Comfort and Function in Patients With Low Vision Using Acuvue Oasys

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05829135
Enrollment
0
Registered
2023-04-25
Start date
2023-05-01
Completion date
2025-06-16
Last updated
2025-06-19

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

Conditions

Low Vision, Photophobia, Visual Impairment

Brief summary

To assess the use of contact lenses with transitions technology to improve glare, light sensitivity and overall visual comfort in patients with visual impairment.

Detailed description

Acuvue Oasys Contact Lenses with Transitions Light Intelligent Technology can adapt to the amount of visible light in the environment, darkening the lenses in bright sunlight, and returning to regular tint in normal or dim environment. Purpose of this study is to assess whether individuals with visual impairment may benefit from these lenses to minimize glare, light sensitivity symptoms and improve the overall visual comfort.

Interventions

DEVICEAcuvue Oasys with Transitions

soft contact lenses with darkening technology

Sponsors

American Academy of Optometry
CollaboratorOTHER
Nova Southeastern University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 64 Years
Healthy volunteers
No

Inclusion criteria

* Ability to give informed consent * Able to speak and read English * Experience glare and light sensitivity that impacts patient's daily living activities * Have confirmed diagnosis of ocular condition including but not limited to Stargardt's, Cone dystrophy, Cone-rod dystrophy, Albinism, Retinitis Pigmentosa and Achromatopsia. * Willing and able to wear the contact lenses as instructed

Exclusion criteria

* Are pregnant, nursing or planning to become pregnant during the course of the study * Have current/recent ocular infection, inflammation, surgery in the past 3 months that contraindicates contact lens wear

Design outcomes

Primary

MeasureTime frameDescription
Glare testMeasure change from baseline at the 6 week follow-up visitMeasure visual acuity and contrast sensitivity with or without illumination source

Secondary

MeasureTime frameDescription
Visual Activities Questionnaire on Glare and Light sensitivity visual functionsMeasure change from baseline at the 6 week follow-up visitPatient will rate 7 questions on scale ranges from 1-5, higher score indicates more symptoms related to glare and light sensitivity during daily living tasks. Max value 35

Countries

United States

Outcome results

None listed

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