Primary Hyperoxaluria Mutation Genotyping

Completed

Conditions studied: Primary Hyperoxaluria

In brief

This study will help us determine whether certain genetic mutations, more than others, are a cause of more severe disease in Primary Hyperoxaluria.

Key facts

Study ID

NCT00589225

Run by

Mayo Clinic

People needed

902

Starts

2003-12-01

Expected to finish

2014-09-01

Last updated by the study team

2016-07-07

Who can join

Age: any. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• You have been diagnosed, or you are in the process of being diagnosed Primary Hyperoxaluria
• You have a family member diagnosed with Primary Hyperoxaluria

Where it is running

• Mayo Clinic — Rochester, Minnesota, United States

Full record on ClinicalTrials.gov

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