Clin2
NCT07729982Possibly a fitRecruiting

Study tracking vision changes in OPA1 optic atrophy

OPA1 Gene MutationOptic Atrophy, Autosomal Dominant

Part of Brain & nervous system, Eyes & vision, Genetic & congenital, Hormones & metabolism clinical trials.

This study follows people with a genetic form of optic atrophy over time to understand how vision changes. It does not test a treatment but helps doctors learn more about the condition to improve care.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
50 people
Ages
Any age
Study type
Observational

Who can take part

  • You are 6 years old or older
  • You have been diagnosed with optic atrophy (damage to the nerve connecting your eye to your brain)
  • You have a confirmed change in the OPA1 gene that causes your condition
  • You or your parent/guardian can understand the study and agree to take part

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

Similar studies

Other trials that look related to this one.

NCT06970106Recruiting· Phase 1/Phase 2
Study of PYC-001 eye injections for people with a type of inherited optic nerve disease

This trial tests a new medicine called PYC-001, given as an injection into the eye, for people with a specific genetic form of vision loss called autosomal dominant optic atrophy (ADOA). It aims to see if the treatment is safe and could help protect or improve vision.

Sydney, New South Wales
NCT06827535Enrolling by invitation
Long-term study of eye changes in glaucoma and high eye pressure

This study tracks changes in blood flow, structure, and vision over time in people with glaucoma or high eye pressure. It aims to understand how these conditions progress, which could help improve future treatment.

Milan, Italy
NCT06682819Recruiting
Looking at eye nerve layers in NOHL gene carriers

This study uses a special eye scan (OCT) to look at the layer of nerve fibers in the retina of people who carry (or don't carry) a specific gene change linked to Leber Hereditary Optic Neuropathy (NOHL). The goal is to find early warning signs in the blood that might show who is at risk of losing vision.

Paris, Paris
NCT06435000Recruiting
A study tracking Stargardt disease progression

This study follows people with Stargardt disease (a genetic eye condition that causes vision loss) over time. It aims to learn more about how the disease progresses and does not test any treatment.

San Diego, California
NCT06375239Recruiting
Study of tests for tracking vision in retinal disease

This study will check if certain vision tests work well in people with retinal diseases like retinitis pigmentosa or Stargardt. Results will help design future trials.

Irvine, California
NCT07425535Recruiting· Early Phase 1
Optic nerve strain study for people without glaucoma

This study looks at how the optic nerve (the part of your eye that sends images to your brain) strains or bends in people who do not have glaucoma. It uses advanced eye imaging and home pressure checks to understand the nerve's health.

Baltimore, Maryland

Hear when a new OPA1 Gene Mutation trial opens

We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.