Improving visual comfort for patients with visual impairment using special contact lenses
Managing Visual Comfort and Function in Patients With Low Vision Using Acuvue Oasys
NA · Nova Southeastern University · NCT05829135
This study is testing special contact lenses that change with light to see if they can make daily life easier for people with visual impairments.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 16 (estimated) |
| Ages | 18 Years to 64 Years |
| Sex | All |
| Sponsor | Nova Southeastern University (other) |
| Locations | 1 site (Davie, Florida) |
| Trial ID | NCT05829135 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of Acuvue Oasys Contact Lenses with Transitions Light Intelligent Technology in enhancing visual comfort for individuals with visual impairments. The lenses are designed to adapt to varying light conditions, reducing glare and light sensitivity. Participants will be assessed to determine if these lenses can significantly improve their daily living activities affected by visual discomfort. The study aims to provide insights into how adaptive lens technology can benefit those with specific ocular conditions.
Who should consider this trial
Good fit: Ideal candidates include individuals with a confirmed diagnosis of ocular conditions such as Stargardt's, Cone dystrophy, or Retinitis Pigmentosa who experience glare and light sensitivity.
Not a fit: Patients who are pregnant, nursing, or have recent ocular infections or surgeries may not benefit from this study.
Why it matters
Potential benefit: If successful, this could significantly enhance the quality of life for patients suffering from visual impairments by reducing glare and improving visual comfort.
How similar studies have performed: While the specific use of these lenses for visual impairment is novel, similar adaptive lens technologies have shown promise in improving visual comfort in other populations.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
Davie, Florida
- Nova Southeastern University — Davie, Florida, United States (RECRUITING)
Study contacts
- Study coordinator: So Yeon Lee, OD
- Email: slee@nova.edu
- Phone: 9542624200
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Photophobia, Visual Impairment, Low Vision