An Observational Study of Japanese Participants With X-linked Retinitis Pigmentosa
NCT04868916 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 15
Last updated 2025-04-25
Summary
The purpose of the study is to identify a cohort of Japanese participants with X-linked retinitis pigmentosa (XLRP) associated with pathogenic variants in the retinitis pigmentosa GTPase regulator (RPGR) gene and to investigate their associated phenotype.
Conditions
- X-Linked Retinitis Pigmentosa
Sponsors & Collaborators
-
Janssen Pharmaceutical K.K.
lead INDUSTRY
Principal Investigators
-
Janssen Pharmaceutical K.K., Japan Clinical Trial · Janssen Pharmaceutical K.K.
Eligibility
- Min Age
- 5 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2021-07-26
- Primary Completion
- 2024-04-23
- Completion
- 2024-04-23
Countries
- Japan
Study Locations
More Related Trials
-
Clinical Implication of Retinitis Pigmentosa Molecular Diagnostic Using High Throughput Sequencing.
NCT02860520 ·Status: UNKNOWN
-
A Natural History Study to Evaluate Functional and Anatomical Progression in Retinitis Pigmentosa
NCT04558983 ·Status: TERMINATED
-
Genetic Study of Patients Suffering From Congenital Amaurosis of Leber or From an Early Severe Retinal Dystrophy
NCT00422721 ·Status: COMPLETED ·Phase: NA
-
InsightRP2 Registry
NCT06982417 ·Status: RECRUITING
-
In Depth Observational Clinical Trial Of Retinitis Pigmentosa Patients
NCT05849987 ·Status: NOT_YET_RECRUITING
-
Retinal Imaging by Adaptive Optics in Healthy Eyes and During Retinal and General Diseases
NCT01546181 ·Status: COMPLETED
-
10-year Progression of Diabetic Retinopathy: Identification of Signs and Surrogate Outcomes
NCT04650165 ·Status: COMPLETED
-
RPE Characterisation With Transscleral Optical Phase Imaging in Retinal Disorders
NCT04912622 ·Status: COMPLETED ·Phase: NA
-
Prospective Exploratory Cohort Study on Ganglion Cell Degeneration in Retinitis Pigmentosa Patients
NCT07056738 ·Status: ENROLLING_BY_INVITATION
-
Prospective Natural History Study of Retinitis Pigmentosa
NCT04285398 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Natural History of Patients With Inherited Retinal Diseases Due to Mutations in RPE65 Gene
NCT04525261 ·Status: COMPLETED
-
Biomarkers in Retinitis Pigmentosa
NCT06306690 ·Status: RECRUITING
-
Multi-center Observation of the Natural Course of Inherited Retinal Dystrophies
NCT03691168 ·Status: UNKNOWN
-
Registry for Severe ROP and Treatment on Visual Outcomes
NCT01559571 ·Status: COMPLETED
-
Global Patient Registry of Inherited Retinal Diseases
NCT05957276 ·Status: ACTIVE_NOT_RECRUITING
-
A New Diagnostic Paradigm for Retinitis Pigmentosa Secondary to USH2A Pathogenic Variants
NCT06545253 ·Status: NOT_YET_RECRUITING
-
Optical Coherence Tomography Angiography in Subjects With Retinal Vascular Disease
NCT04505618 ·Status: RECRUITING ·Phase: NA
-
Natural History and Risk Factors of TAO
NCT03515863 ·Status: UNKNOWN
-
Micropulse Laser for Geographic Atrophy
NCT01799564 ·Status: COMPLETED ·Phase: NA
-
High Myopia: Extended and Longterm Observation of Pathologic Myopia Patients With the Risk for Developing a Myopic Choroidal Neovascularization (CNV)
NCT03070717 ·Status: COMPLETED
-
Gene Expression in Patients With Epiretinal Membranes
NCT01946451 ·Status: UNKNOWN
-
Natural History Study of Patients With Leber Congenital Amaurosis Associated With Mutations in RPE65
NCT02714816 ·Status: COMPLETED
-
Development of Visual Function Evaluation Method
NCT03281005 ·Status: COMPLETED
-
Heredity of Retinal Vessel Tortuosity
NCT00427063 ·Status: COMPLETED
-
Natural History Study of Patients With EYS-Associated RP
NCT07228793 ·Status: RECRUITING