Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 3:18 AM
Ignite Modification Date:
2025-12-25 @ 3:18 AM
NCT ID:
NCT02983305
Eligibility Criteria:
Inclusion criteria for subjects with retinal dystrophy:
* diagnosis of retinal dystrophy
* severe vision loss that constitutes legal blindness
* able to perform a reliable Goldmann visual field test
* constricted visual field less than or equal to 20 degrees by Goldmann perimetry using the III4e stimulus in at least one eye with best-corrected visual acuity ≥ 20/60
Inclusion criteria for control subjects:
* healthy controls
* visit history with the Comprehensive and Pediatric Ophthalmology Services at the University of Michigan
* able to perform a reliable Goldmann visual field test
Exclusion criteria for subjects with retinal dystrophy:
* movement disorder that precludes evaluation of mobility
* functional vision loss
* pregnant women
Exclusion criteria for control subjects:
* visually significant ocular condition other than correctable refractive error
* movement disorder that precludes evaluation of mobility
* functional vision loss
* pregnant women
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
12 Years
Study:
NCT02983305
Study Brief:
Protocol Section:
NCT02983305