Status:
UNKNOWN
Mobility Protocol Adapted for Advanced Visually Impaired Subjects
Lead Sponsor:
Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts
Conditions:
Pigmentary Retinopathy
Eligibility:
All Genders
18-75 years
Phase:
NA
Brief Summary
Retinitis Pigmentosa is characterized by a progressive disappearance of photoreceptors, responsible for a progressive and severe loss of vision. People Retinitis Pigmentosa therefore encounter a larg...
Detailed Description
This is monocentric study and the total duration of the study is 48 months. The duration of participation for each research subject is 3 months and maximum 4 visits. This is research involving the hum...
Eligibility Criteria
Inclusion
- Retinitis Pigmentosa, non-syndromic, the diagnosis of which has been confirmed by an ophtmalmologist
- ETDRS visual acuity less than 2/10 (\>+0.7 logMAR; \<20/100 Snellen)
- Doesn't participate in clinical research that may interfere with this study
- Sufficient knowledge of the French language to ensure a perfect understanding of the tasks to be performed and the instructions received
- Consent to the study signed after information by the investigator
- Health insurance affiliation
Exclusion
- Pregnant women
- Inability to give personal consent
- Cataract surgery in the 3 months preceding inclusion
- Amblyopia
- Inability to comply with the instructions for carrying out the study tasks or to complete the study visits
- MMSE score without visual item ≤ 20/25
- Drug treatment which can lead to motor, visual or cognitive disorders (PSA, neuroleptics,etc.) or which may interfere with the study's evaluations
Key Trial Info
Start Date :
March 2 2020
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
June 4 2024
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT04419285
Start Date
March 2 2020
End Date
June 4 2024
Last Update
June 5 2020
Active Locations (1)
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1
Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts
Paris, France, 75012