Dent Disease Clinical Trial
Official title:
Screening for Dent Disease Mutations in Patients With Proteinuria
Verified date | April 2020 |
Source | Mayo Clinic |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study will help the investigator determine whether certain genetic mutations, more than others, are a cause of more severe disease in Dent Disease.
Status | Completed |
Enrollment | 180 |
Est. completion date | July 2019 |
Est. primary completion date | July 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | N/A and older |
Eligibility |
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 |
Country | Name | City | State |
---|---|---|---|
United States | Mayo Clinic | Rochester | Minnesota |
Lead Sponsor | Collaborator |
---|---|
Mayo Clinic | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of subjects with genetic mutations in either the CLCN5 or ORCL1 gene | 4 years |
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