Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
20 participants
OBSERVATIONAL
2013-10-31
2015-09-30
Brief Summary
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Detailed Description
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* Sign a consent form indicating the patient's willingness to participate.
* Provide a signed medical release form allowing the investigator to request your official kidney biopsy reports, and also allowing the investigator to request the original slides for review. At the end of the study, all slides will be returned to the referring facility.
* The investigator will also review your medical record
Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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Dent Disease patients
Patients with diagnosed Dent Disease
Renal Biopsy
Interventions
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Renal Biopsy
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
MALE
No
Sponsors
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Mayo Clinic
OTHER
Responsible Party
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John Lieske
M.D.
Principal Investigators
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John C Lieske, M.D.
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic
Locations
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Mayo Clinic
Rochester, Minnesota, United States
Countries
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Related Links
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Rare Kidney Stone Consortium
Other Identifiers
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13-003738
Identifier Type: -
Identifier Source: org_study_id
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