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North American Mitochondrial Disease Consortium Patient Registry and Biorepository (NAMDC)

RECRUITINGSponsored by Columbia University
Actively Recruiting
SponsorColumbia University
Started2011-01-31
Est. completion2026-12-31
Eligibility
Healthy vol.Accepted
Locations16 sites
View on ClinicalTrials.gov →

NCT01694940

Summary

The North American Mitochondrial Disease Consortium (NAMDC) maintains a patient contact registry and tissue biorepository for patients with mitochondrial disorders.

Eligibility

Healthy volunteers accepted
Inclusion Criteria:

* Patients diagnosed with or suspected to have a mitochondrial disorder
* Adult carriers of known mitochondrial DNA mutations
* Patients with laboratory analysis indicative of a mitochondrial disorder.
* Medical information and tissue samples are also accepted from deceased individuals who fulfill the above criteria.

Exclusion Criteria:

* Patients not suspected of having a mitochondrial disorder
* Patients not suspected of carrying a mitochondrial DNA or nuclear DNA mutation that affects mitochondrial function.

Conditions7

Deletion and Duplication of Mitochondrial DNADiabetesDisorder of Mitochondrial Respiratory Chain ComplexesHeart DiseaseMitochondrial DiseasesMitochondrial DisordersMitochondrial Genetic Disorders

Locations16 sites

University of California San Diego
San Diego, California, 92103
Richard Hass, MD18588226700rhass@ucsd.edu
Lucile Packard Children's Hospital
Stanford, California, 94305
Gregory Enns, MD1-650-723-6858
Children's Hospital of Colorado
Aurora, Colorado, 80045
Johan Van Hove, MD PhD MBA3037242351
Children's National Medical Center
Washington D.C., District of Columbia, 20010
Andrea Gropman, MD202-476-3511agropman@cnmc.org
University of Florida
Gainsville, Florida, 32610
Peter Stacpole, MD13522658909stacpool@gcrc.ufl.edu

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