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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
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

Full criteria on ClinicalTrials.gov

Sites (14)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hospital for Sick Children
Coordinator of this site? Confirm its status
TorontoCanadaUnknown status
University of Tübingen
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TübingenGermanyUnknown status
Centre Hospitalier National D'ophtalmologie Des Quinze Vingts
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ParisFranceUnknown status
Moorfields Eye Hospital
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LondonUnited KingdomUnknown status
Radboud University
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NijmegenNetherlandsUnknown status
Kellogg Eye Center, University of Michigan
Coordinator of this site? Confirm its status
Ann ArborUnited StatesUnknown status
Wilmer Eye Institute at Johns Hopkins
Coordinator of this site? Confirm its status
BaltimoreUnited StatesUnknown status
Massachusetts Eye and Ear
Coordinator of this site? Confirm its status
BostonUnited StatesUnknown status
Retina Foundation of the Southwest
Coordinator of this site? Confirm its status
DallasUnited StatesUnknown status
Vitreo Retinal Associates
Coordinator of this site? Confirm its status
GainesvilleUnited StatesUnknown status
Baylor Eye Physicians and Surgeons
Coordinator of this site? Confirm its status
HoustonUnited StatesUnknown status
OHSU Casey Eye Institute
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PortlandUnited StatesUnknown status
Moran Eye Center, University of Utah
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Salt Lake CityUnited StatesUnknown status
University of California San Francisco
Coordinator of this site? Confirm its status
San FranciscoUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.