CompletedNot Applicable

Dent Disease Mutation Genotyping

United States180 participantsStarted 2012-08

Plain-language summary

This study will help the investigator determine whether certain genetic mutations, more than others, are a cause of more severe disease in Dent Disease.

Who can participate

SexALL

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Inclusion Criteria: * The patient has been diagnosed, or in the process of being diagnosed with Dent Disease. * The patient has a family member diagnosed with Dent Disease. Exclusion Criteria: \- None

What they're measuring

Number of subjects with genetic mutations in either the CLCN5 or ORCL1 gene

Timeframe: 4 years

Trial details

NCT IDNCT01783795

SponsorMayo Clinic

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2019-07

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