Inherited Retinal Degenerative Disease Registry — MRTR  

Retinitis Pigmentosa Clinical Trial

Official title: Foundation Fighting Blindness My Retina Tracker Registry

Status Recruiting

Clinical Trial Summary

The My Retina Tracker® Registry is sponsored by the Foundation Fighting Blindness and is for people affected by one of the rare inherited retinal degenerative diseases studied by the Foundation. It is a patient-initiated registry accessible via a secure on-line portal at www.MyRetinaTracker.org. Affected individuals who register are guided to create a profile that captures their perspective on their retinal disease and its progress; family history; genetic testing results; preventive measures; general health and interest in participation in research studies. The participants may also choose to ask their clinician to add clinical measurements and results at each clinical visit. Participants are urged to update the information regularly to create longitudinal records of their disease, from their own perspective, and their clinical progress. The overall goals of the Registry are: to better understand the diversity within the inherited retinal degenerative diseases; to understand the prevalence of the different diseases and gene variants; to assist in the establishment of genotype-phenotype relationships; to help understand the natural history of the diseases; to help accelerate research and development of clinical trials for treatments; and to provide a tool to investigators that can assist with recruitment for research studies and clinical trials.

Clinical Trial Description

My Retina Tracker Registry provides two portals for data entry and review. Initial registration in the My Retina Tracker Registry is initiated by a participant, not a clinician. Using the participant portal, the participant establishes a username and password, is guided through on-line informed consent, and can then use an interactive guide to record their ophthalmic and family history, genotype and other subjective diagnosis-related and general health information. Drop-down menus and standardized vocabulary are used for database consistency. They may also attach documents, such as medical records, to maintain their personal medical files on their disease. Participants are encouraged to update their profiles regularly to create a longitudinal history of their disease. Participants can see aggregated data for all other participants in the registry and compare their own disease and status to others.

After a profile has been established, Registry members may ask their clinician or genetic counselor to add specific ophthalmic exam and measurement results to the profile. This is done through the clinical portal which also uses a series of drop-down menus to expedite entry and standardize data. Clinicians cannot see the participant data when adding the clinical exam data. Participants are encouraged to collect this data at each medical exam, to create a longitudinal clinical data set.

Access to de-identified data or study recruitment assistance is available to qualified investigators who may inquire by contacting Coordinator@MyRetinaTracker.org. A process that maintains patient anonymity and privacy protection, exists for researchers with Institutional Review Board-approved projects who wish to contact registry participants of interest. ;

Related Conditions & MeSH terms

• Abetalipoproteinemia
• Achromatopsia
• Bardet-Biedl Syndrome
• Bassen-Kornzweig Syndrome
• Batten Disease
• Best Disease
• Blindness
• Choroidal Dystrophy
• Choroideremia
• Color Vision Defects
• Cone Dystrophy
• Cone-Rod Dystrophy
• Congenital Stationary Night Blindness
• Enhanced S-Cone Syndrome
• Eye Diseases
• Eye Diseases Hereditary
• Eye Diseases, Hereditary
• Fundus Albipunctatus
• Goldmann-Favre Syndrome
• Gyrate Atrophy
• Juvenile Macular Degeneration
• Kearns-Sayre Syndrome
• Leber Congenital Amaurosis
• Macular Degeneration
• Neuronal Ceroid-Lipofuscinoses
• Night Blindness
• Refsum Disease
• Refsum Syndrome
• Retinal Disease
• Retinal Diseases
• Retinitis
• Retinitis Pigmentosa
• Retinitis Punctata Albescens
• Retinoschisis
• Rod Dystrophy
• Rod Monochromacy
• Rod-Cone Dystrophy
• Stargardt Disease
• Syndrome
• Usher Syndrome
• Usher Syndromes
• Vitamin A Deficiency

• NCT number: NCT02435940
• Study type: Observational [Patient Registry]
• Source: Foundation Fighting Blindness
• Contact: Registry Coordinator
• Phone: 800-683-5555
• Email: Coordinator@MyRetinaTracker.org
• Status: Recruiting
• Start date: June 2014
• Completion date: June 2037