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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01644552
Other study ID # 1004M80112
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 2010
Est. completion date September 2011

Study information

Verified date October 2019
Source University of Minnesota
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Patients with aniridia have positive angle kappas.


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date September 2011
Est. primary completion date September 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 1 Month to 85 Years
Eligibility Inclusion Criteria:

- patients with aniridia only

Exclusion Criteria:

- poor va

- PK,

- K-pro

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States University of Minnesota Dept of ophthalmlogy Minneapolis Minnesota

Sponsors (1)

Lead Sponsor Collaborator
University of Minnesota

Country where clinical trial is conducted

United States, 

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