What this study is
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.
Study details
- Official title
- Foundation Fighting Blindness My Retina Tracker Registry
- Sponsor
- Foundation Fighting Blindness
- Conditions
- Eye Diseases Hereditary · Retinal Disease · Achromatopsia · Bardet-Biedl Syndrome · Bassen-Kornzweig Syndrome · Batten Disease · Best Disease · Choroidal Dystrophy · Choroideremia · Cone Dystrophy · Cone-Rod Dystrophy · Congenital Stationary Night Blindness · Enhanced S-Cone Syndrome · Fundus Albipunctatus · Goldmann-Favre Syndrome · Gyrate Atrophy · Juvenile Macular Degeneration · Kearns-Sayre Syndrome · Leber Congenital Amaurosis · Refsum Syndrome · Retinitis Pigmentosa · Retinitis Punctata Albescens · Retinoschisis · Rod-Cone Dystrophy · Rod Dystrophy · Rod Monochromacy · Stargardt Disease · Usher Syndrome
- Enrolling
- 20,000 people
- Starts
- 2014-06
- Est. completion
- 2037-06
- Record
- View on ClinicalTrials.gov ↗
Who can join
Sex ALLHealthy volunteers AcceptedYou may qualify if
- Diagnosed with an inherited retinal degenerative disease OR
You can't join if
- Glaucoma only
- Diabetic retinopathy only
- Non-retinal disease
- Not heritable retinal disease
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (1)
1 openFoundation Fighting Blindness
Columbia, Maryland, United States
- Registry Coordinator · Contact800-683-5555 ext. 1594Coordinator@MyRetinaTracker.org
- Todd Durham, PhD · Principal investigator
Recruiting
Study team
Sponsor
Foundation Fighting Blindness
Study ID FFB-Registry-01
Principal investigator
Todd Durham, PhD
Senior Vice President, Clinical and Outcomes Research
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.