Trials / Enrolling By Invitation
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.