NCT03146078Active, not recruiting
Rate of Progression in USH2A-related Retinal Degeneration
Source: ClinicalTrials.gov · Last updated 29 Oct 2026
Brief summary (registry, in English)
The overall goal of this project funded by the Foundation Fighting Blindness is to characterize the natural history of disease progression in patients with USH2A related retinal degeneration associated with congenital hearing loss (Usher syndrome type 2a) or non-syndromic retinitis pigmentosa (RP39). RUSH2A Extension Study: The purpose of this addendum is to extend RUSH2A to 7- and 9-year visits, with the goal to use longer term data to further develop and support early candidate endpoints as possible clinical trial outcomes.
- Status (registry)
- Active, not recruiting
- Study type
- Observational
- Enrollment
- 127 (actual)
- First submitted
- 4 May 2017
- Start date
- 11 Aug 2017
- Primary completion date
- 28 Apr 2023
- Lead sponsor
- Jaeb Center for Health Research
- Diseases
- Retinitis pigmentosa
- NCT number
- NCT03146078
What you commit to
- Study type: Observational
- Participants enrolled: 127
- From 11 Aug 2017 to the primary completion date, 28 Apr 2023
- 14 sites in 6 countries
- 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.
Prior treatment
- Current or any history of (e.g., prior to cataract or refractive surgery) spherical equivalent of the refractive error worse than -8 Diopters of myopia
- Expected to have cataract removal surgery during the study
Other illness
- History of more than 1 year of cumulative treatment, at any time, with an agent associated with pigmentary retinopathy (including hydroxychloroquine, chloroquine, thioridazine, and deferoxamine)
- Ocular Exclusion Criteria
- If either eye has any of the following, the patient is not eligible:
- Current vitreous hemorrhage
- Current or any history of rhegmatogenous retinal detachment
- History of intraocular surgery (e.g., cataract surgery, vitrectomy, penetrating keratoplasty, or LASIK) within the last 3 months
- Current or any history of confirmed diagnosis of glaucoma (e.g., based on glaucoma visual field, nerve changes, or glaucoma filtering surgery)
- Current or any history of retinal vascular occlusion or proliferative diabetic retinopathy
- History or current evidence of ocular disease that, in the opinion of the investigator, may confound assessment of visual function
- History of treatment for retinitis pigmentosa that could affect the progression of retinal degeneration (including participation in a clinical trial within the last year or a retained drug delivery device)
Other
- Mutations in genes that cause autosomal dominant RP, X-linked RP, or presence of biallelic mutations in autosomal recessive RP/retinal dystrophy genes other than USH2A
- Expected to enter experimental treatment trial at any time during this study
Who the study is looking for
- Willing and able to complete the informed consent process
- Ability to return for all study visits over 48 months if in the natural history study
- Age ≥ 8 years
- At least 2 pathogenic or likely pathogenic mutations in USH2A gene from a clinically certified lab report
- Ocular Inclusion Criteria
- Both eyes must meet all of the following:
- Clinical diagnosis of a rod-cone degeneration
- Clear ocular media and adequate pupil dilation to permit good quality photographic imaging
- Ability to perform kinetic and static perimetry reliably
Age in the registry: 8 years to - · Sex: All · Does not accept healthy volunteers
Sites (14)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Hospital for Sick Children Coordinator of this site? Confirm its status | Toronto | Canada | Unknown status |
| University of Tübingen Coordinator of this site? Confirm its status | Tübingen | Germany | Unknown status |
| Centre Hospitalier National D'ophtalmologie Des Quinze Vingts Coordinator of this site? Confirm its status | Paris | France | Unknown status |
| Moorfields Eye Hospital Coordinator of this site? Confirm its status | London | United Kingdom | Unknown status |
| Radboud University Coordinator of this site? Confirm its status | Nijmegen | Netherlands | Unknown status |
| Kellogg Eye Center, University of Michigan Coordinator of this site? Confirm its status | Ann Arbor | United States | Unknown status |
| Wilmer Eye Institute at Johns Hopkins Coordinator of this site? Confirm its status | Baltimore | United States | Unknown status |
| Massachusetts Eye and Ear Coordinator of this site? Confirm its status | Boston | United States | Unknown status |
| Retina Foundation of the Southwest Coordinator of this site? Confirm its status | Dallas | United States | Unknown status |
| Vitreo Retinal Associates Coordinator of this site? Confirm its status | Gainesville | United States | Unknown status |
| Baylor Eye Physicians and Surgeons Coordinator of this site? Confirm its status | Houston | United States | Unknown status |
| OHSU Casey Eye Institute Coordinator of this site? Confirm its status | Portland | United States | Unknown status |
| Moran Eye Center, University of Utah Coordinator of this site? Confirm its status | Salt Lake City | United States | Unknown status |
| University of California San Francisco Coordinator of this site? Confirm its status | San Francisco | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.