Gyrate Atrophy of the Choroid and Retina

Plain-language summary

This study examined an inherited eye disease called gyrate atrophy of the choroid and retina. People with high blood ornithine levels (hyperornithinemia) and a deficiency of the OAT enzyme could take part. It was carried out as a study with no assigned phase and has been completed.

The summary above is a plain-language rendering of the official record. The original English title is shown for reference.

Trial details

Phase

N/A

Status

Completed

Sponsor

National Eye Institute (NEI)

Start date

1/1/1978

Estimated completion

3/1/2004

Countries

United States

Related genes

Locations

• Bethesda, United States

Eligibility criteria

Criteria are reproduced from the ClinicalTrials.gov record in the original English. Only the trial team can determine eligibility.

INCLUSION CRITERIA:

Patients must have hyperornithemia and a deficiency of OAT activity to enter the study.