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Rare and Undiagnosed Disease Research Biorepository — PRaUD  

Rare Diseases Clinical Trial

Official title:
Rare and Undiagnosed Disease Research Biorepository

Clinical Trial Summary

This research study is being done to find markers and identify causes of rare and undiagnosed diseases by analyzing patient's DNA (i.e., genetic material), RNA, plasma, urine, tissues, or other samples that could be informative of symptoms. Researchers are creating a biobank (library) of samples and information to learn more about treating rare and undiagnosed diseases.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04703179
Study type Observational [Patient Registry]
Source Mayo Clinic
Contact
Status Enrolling by invitation
Phase
Start date November 20, 2020
Completion date November 2025
View Details
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