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Advanced Characterization of Autosomal Dominant Optic Atrophy

NCT01522638 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2012-01-31

No results posted yet for this study

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

Sponsors & Collaborators

  • Glostrup University Hospital, Copenhagen

    lead OTHER

Principal Investigators

  • Michael Larsen, MD, Prof. DMSc · Glostrup University Hospital

Eligibility

Min Age
8 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-12-31
Primary Completion
2014-06-30
Completion
2015-06-30

Countries

  • Denmark

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01522638 on ClinicalTrials.gov