Last updated: June 16, 2023
Sponsor: Massachusetts Eye and Ear Infirmary
Overall Status: Completed
Phase
N/A
Condition
Eye Disorders/infections
Vision Loss
Blurred Vision
Treatment
Bilateral monocular visual confusion (bilateral see-through)
Unilateral monocular visual confusion (unilateral see-through)
Binocular visual confusion (unilateral opaque)
Clinical Study ID
NCT04957745
2021P001757
R01EY031777
Ages > 14 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Better than 20/40 visual acuity in the worse eye
- No restrictions of the peripheral visual field: (at least 60 degrees vertically and 40degrees horizontally)
- At least 14 years of age (no upper age limit)
- Able to give voluntary, informed consent
- Able to understand English
- Binocular vision parameters within normal limits (Stereopsis ≤ 100 arc sec on anystereo test)
Exclusion
Exclusion criteria:
- Patients with any physical or mental disabilities, including cognitive dysfunction,balance problems, or other deficits that could impair their ability to respond to thestimuli presented in this study will be excluded
- Being unable to complete sessions lasting 2-3 hours
Study Design
Total Participants: 13
Treatment Group(s): 3
Primary Treatment: Bilateral monocular visual confusion (bilateral see-through)
Phase:
Study Start date:
November 09, 2021
Estimated Completion Date:
July 27, 2022
Connect with a study center
Schepens Eye Research Institute
Boston, Massachusetts 02114
United StatesSite Not Available

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