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Clinical Trial Summary

This study is being done to obtain pathology reports from all patients in the Dent disease registry who have had a kidney biopsy. The investigator will collect the biopsy slides and reports in an attempt to determine if they have any common findings.


Clinical Trial Description

If the patient agrees to be in the study, the patient will be asked to participate in the following:

- 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 ;


Study Design

Observational Model: Cohort, Time Perspective: Retrospective


Related Conditions & MeSH terms


NCT number NCT02022189
Study type Observational
Source Mayo Clinic
Contact
Status Completed
Phase N/A
Start date October 2013
Completion date September 2015

See also
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