NCT02435940Recruiting
Inherited Retinal Degenerative Disease Registry
Foundation Fighting Blindness My Retina Tracker Registry
Source: ClinicalTrials.gov · Last updated 19 May 2026
Brief summary (registry, in English)
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.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 20000 (estimated)
- First submitted
- 3 Apr 2015
- Start date
- 1 Jun 2014
- Primary completion date
- 30 Jun 2037
- Lead sponsor
- Foundation Fighting Blindness
- Diseases
- Macular degeneration, Retinitis pigmentosa
- NCT number
- NCT02435940
What you commit to
- Study type: Observational
- Planned participants: 20000
- From 1 Jun 2014 to the primary completion date, 30 Jun 2037
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Non-retinal disease
- Not heritable retinal disease
Other
- Glaucoma only
- Diabetic retinopathy only
Who the study is looking for
- Diagnosed with an inherited retinal degenerative disease OR
Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Foundation Fighting Blindness Coordinator of this site? Confirm its status | Columbia | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.