A Novel Mutation of the Spectrin Gene

Completed

Conditions studied: Hereditary Elliptocytosis (HE), Hereditary Pyropoikilocytosis (HPP)

In brief

The purpose of this study is to find a gene or its mutation (an altered gene) that puts individuals at risk for developing HE or HPP.

Key facts

Study ID

NCT00723567

Run by

University of Utah

People needed

12

Starts

2008-02-01

Expected to finish

2008-12-01

Last updated by the study team

2009-02-19

Who can join

Age: 7 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• > 7 years of age
• Consenting family members

You may not qualify if…

• Anyone not meeting the criteria above

Where it is running

• University of Utah — Salt Lake City, Utah, United States

Full record on ClinicalTrials.gov

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