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 @ 2:12 AM
Ignite Modification Date:
2025-12-25 @ 2:12 AM
NCT ID:
NCT04448860
Eligibility Criteria:
Inclusion Criteria:
* Gender male or female
* Non-syndromic pigmentary retinopathy: diagnosis confirmed by a specialist (RP patients)
* Pigmentary retinopathy with different damage's levels of visual field, acuity and sensitivity to contrasts (RP patients)
* Visual acuity of both corrected eyes (glasses, lenses) greater than or equal to 8/10 (or ≤ 0.1 logMAR) (Healthy volounteers)
* Normal semi-automated kinetic visual field (Healthy volounteers)
* Not participating in any other clinical trial that may interfere with this study
* Sufficient knowledge of the French language to ensure understanding of the tasks to be performed and the instructions received
* Social insurance
* Consent signed after information by the investigator
Exclusion Criteria:
* Pregnant woman
* Inability to give personal consent
* Cataract surgery in the 3 months before inclusion
* Amblyopia
* Inability to comply with the instructions for the study tasks or to complete the study visits
* MMSE score without visual item ≤ 20/25 for RP patients
* MMSE score with visual item ≤ 25/30 for healthy volunteers
* Drug treatment which may cause motor, visual or cognitive disorders (neuroleptics, etc.) or which may interfere with study evaluations
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
75 Years
Study:
NCT04448860
Study Brief:
Protocol Section:
NCT04448860