Trials / Enrolling By Invitation
Enrolling By InvitationNCT01803906
Tissue Sample Study for Mitochondrial Disorders
Tissue Study for Mitochondrial Disorders
- Status
- Enrolling By Invitation
- Phase
- —
- Study type
- Observational
- Enrollment
- 6,900 (estimated)
- Sponsor
- Columbia University · Academic / Other
- Sex
- All
- Age
- —
- Healthy volunteers
- Accepted
Summary
The investigators are studying patients with undefined mitochondrial diseases to identify genetic mutations in nuclear or mitochondrial Deoxyribonucleic Acid (DNA). Most patients with suspected or known mitochondrial diseases have no genetic confirmation. The investigators expect that evaluating tissue samples from patients with mitochondrial disorders will lead us to discover mutations in new or known genes causing mitochondrial dysfunction.
Detailed description
Presently, the investigators know of about 200 mitochondrial disorders. The investigators know that there are about 1,300 genes responsible for mitochondrial function. Thus, there are a lot of mutated genes to be discovered out there. Currently, most patients with suspected or known mitochondrial disorders do not have genetic confirmation of the disease. The goal of this project is to perform biochemical and DNA analysis on tissue samples of patients with mitochondrial disorders to find new genes that might be involved in mitochondrial dysfunction. Leftover patient tissue samples will be obtained for analysis from within the Columbia Presbyterian Medical Center. Left over patient samples may also be sent from outside the institution. This is not a "first-step" in the diagnostic process, but rather an option for evaluation in patient samples for which no known diagnosis or genetic confirmation has been made. The research laboratory does not guarantee that a sample will be analyzed. Sample analysis is performed according to research interest. If they choose, patients can be contacted should laboratory findings provide insight into their disease.
Conditions
- Mitochondrial Disorders
- Mitochondrial Disease
- Melas
- Kearns Sayer
- NARP
- MNGIE
- LHON
- Mitochondrial Depletion Syndrome
- Leigh's Disease
Timeline
- Start date
- 2012-02-01
- Primary completion
- 2026-12-01
- Completion
- 2026-12-01
- First posted
- 2013-03-04
- Last updated
- 2026-01-07
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01803906. Inclusion in this directory is not an endorsement.