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Enrolling By InvitationNCT01440218

Idiopathic Diseases of Man

Idiopathic Diseases of Man (IDIOM)

Status
Enrolling By Invitation
Phase
Study type
Observational
Enrollment
10 (estimated)
Sponsor
Scripps Translational Science Institute · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

This research is being done to learn more about possible genetic causes of currently undiagnosed conditions, and to find out how the development of new technologies, such as DNA sequencing, can increase knowledge of the role genetic variants play in disorders and possibly how genetic variants may help de-termine the best treatment options. The recent development of new technologies has increased our ability to understand how genetic mutations are associated with disease. Using these technologies to find the genetic variants responsible for rare diseases is a rapidly growing field and has already begun to transform the way conditions with unknown causes are diagnosed and treated. Hypothesis: Identification of new genomic variants associated with idiopathic diseases and/or diseases of unknown etiology will advance medical knowledge about rare and common diseases.

Conditions

Timeline

Start date
2011-09-01
Primary completion
2025-12-01
Completion
2030-12-01
First posted
2011-09-26
Last updated
2025-01-16

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01440218. Inclusion in this directory is not an endorsement.