Prospective Natural History Study of Retinitis Pigmentosa
NCT04285398 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 82
Last updated 2025-05-22
Summary
This is natural history study of rods and cones degenerations in patients with Retinitis Pigmentosa (RP) caused by pathogenic mutations in RHO, PDE6a or PDE6b gene mutations.
Conditions
Interventions
- OTHER
-
Ophthalmic examinations
Slit-lamp examination, IntraOcular Pressure, Visual Acuity, Visual Field, Full-field Stimulus Threshold, Dark adaptometry, Color Vision testing, Optical Coherence Tomography, Fundus AutoFluorescence and Adaptive Optics imaging.
- OTHER
-
Mobility Test
Functional test to evaluate mobility and postural condition of patients
Sponsors & Collaborators
-
SparingVision
lead INDUSTRY
Principal Investigators
-
Isabelle Audo, MD, PhD · CHNO XV-XX Paris - CIC 1423
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- SCREENING
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2020-02-12
- Primary Completion
- 2026-06-30
- Completion
- 2026-06-30
Countries
- United States
- France
Study Locations
More Related Trials
-
Natural History Study of CEP290-Related Retinal Degeneration
NCT03396042 ·Status: COMPLETED
-
Study of BEST1 Vitelliform Macular Dystrophy
NCT05809635 ·Status: RECRUITING
-
Natural History Study of Patients With EYS-Associated RP
NCT07228793 ·Status: RECRUITING
-
Prospective Exploratory Cohort Study on Ganglion Cell Degeneration in Retinitis Pigmentosa Patients
NCT07056738 ·Status: ENROLLING_BY_INVITATION
-
In Depth Observational Clinical Trial Of Retinitis Pigmentosa Patients
NCT05849987 ·Status: NOT_YET_RECRUITING
-
Longitudinal Prospective Natural History Study of Retinopathy in Zellweger Spectrum Disorder
NCT06190626 ·Status: RECRUITING
-
Natural History Study of Retinitis Pigmentosa Type 11
NCT04805658 ·Status: ACTIVE_NOT_RECRUITING
-
Natural History of Geographic Atrophy Associated With Age-Related Macular Degeneration
NCT02941263 ·Status: COMPLETED
-
An Observational Study of Japanese Participants With X-linked Retinitis Pigmentosa
NCT04868916 ·Status: COMPLETED
-
Retinal Imaging by Adaptive Optics in Healthy Eyes and During Retinal and General Diseases
NCT01546181 ·Status: COMPLETED
-
Multi-center Observation of the Natural Course of Inherited Retinal Dystrophies
NCT03691168 ·Status: UNKNOWN
-
Natural History of Autosomal Dominant Optic Atrophy (ADOA), Caused by OPA1 Mutation
NCT06140329 ·Status: TERMINATED
-
Prevalence of Age Related Macular Degeneration (ARMD) in Parkinson's Patients and Assesment of the Role of L-DOPA
NCT03415984 ·Status: COMPLETED
-
Clinical and Genetic Findings in Patients With PRPF31-associated Retinitis Pigmentosa
NCT06368375 ·Status: COMPLETED
-
PreView PHP Preferential Hyperacuity Perimeter for the Detection of Choroidal Neovascularization
NCT00358345 ·Status: COMPLETED
-
Evaluation of the Protective Role of the L-DOPA Against Age Related Macular Degeneration in Parkinson's Patients
NCT02863640 ·Status: TERMINATED
-
Stargardt-like Macular Dystrophy (STDG3) Secondary to Mutations in ELOVL4
NCT04591483 ·Status: RECRUITING
-
Optical Coherence Tomography and Microperimetry Biomarker Evaluation in Patients With Geographic Atrophy Study
NCT05963646 ·Status: COMPLETED
-
An Observational Study of the Progression of Intermediate Age-Related Macular Degeneration
NCT05300724 ·Status: ACTIVE_NOT_RECRUITING
-
Adaptive Optics Imaging of Outer Retinal Diseases
NCT05355415 ·Status: RECRUITING
-
A Natural History of the Progression of Stargardt Disease: Retrospective and Prospective Studies
NCT01977846 ·Status: COMPLETED
-
A New Diagnostic Paradigm for Retinitis Pigmentosa Secondary to USH2A Pathogenic Variants
NCT06545253 ·Status: NOT_YET_RECRUITING
-
Genetic Study of Patients Suffering From Congenital Amaurosis of Leber or From an Early Severe Retinal Dystrophy
NCT00422721 ·Status: COMPLETED ·Phase: NA
-
Visual Function Tests in Age-related Macular Degeneration
NCT03275753 ·Status: TERMINATED
-
PHP Home Preferential Hyperacuity Perimeter for the Detection of Choroidal Neovascularization (CNV)
NCT00359008 ·Status: COMPLETED