CompletedNot Applicable

Primary Hyperoxaluria Mutation Genotyping

United States902 participantsStarted 2003-12

Plain-language summary

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

Who can participate

SexALL

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Inclusion Criteria: * You have been diagnosed, or you are in the process of being diagnosed Primary Hyperoxaluria * You have a family member diagnosed with Primary Hyperoxaluria

What they're measuring

To determine whether certain genetic mutations, more than others, are a cause of more severe disease in Primary Hyperoxaluria

Timeframe: 2 years

Trial details

NCT IDNCT00589225

SponsorMayo Clinic

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2014-09

View on ClinicalTrials.gov More Primary Hyperoxaluria trials