NCT01522638

Advanced Characterization of Autosomal Dominant Optic Atrophy

Cross Sectional Study of Autosomal Dominant Opticus Atrophy

• Status: Unknown
• Phase: —
• Study type: Observational
• Enrollment: 50 (estimated)
• Sponsor: Glostrup University Hospital, Copenhagen · Academic / Other
• Sex: All
• Age: 8 Years
• Healthy volunteers: Accepted

Summary

The purpose of this study is to determine the anatomy of the retina and the optic nerve in patients with autosomal dominant optic atrophy (ADOA). Based on these findings the aim of the study is to determine why patients with the same type of genetic material, i.e. the same mutation, have such large variations of symptoms, spanning from unaffected subjects to blindness. The project requires examination of both healthy and affected family members.

Conditions

• Optic Atrophy, Autosomal Dominant

Timeline

• Start date: 2011-12-01
• Primary completion: 2014-06-01
• Completion: 2015-06-01
• First posted: 2012-01-31
• Last updated: 2012-01-31

Locations

1 site across 1 country: Denmark