OAT

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Scientists track rare eye disease to uncover clues for future treatments

Knowledge-focused Ongoing

This study follows 46 people with gyrate atrophy, a rare genetic condition that causes vision loss, over 4 years. Researchers measure ornithine levels in the blood and track changes in the retina using eye scans and photos. The goal is to learn how the disease progresses under st…

Matched conditions: OAT

Sponsor: Jaeb Center for Health Research • Aim: Knowledge-focused

Last updated Jun 16, 2026 12:49 UTC

OAT

Get alerted when new OAT trials appear

Scientists track rare eye disease to uncover clues for future treatments