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Clinical Trial Summary

The main goal of the project is provision of a global registry for mitochondrial disorders to harmonize previous national registries, enable world-wide participation and facilitate natural history studies, definition of outcome measures and conduction of clinical trials.


Clinical Trial Description

The global mitochondrial registry and natural history study is part of the EU-financed GENOMIT project, co-ordinated by Dr. Holger Prokisch, Technische Universität München (TUM).It aims at advancing the understanding of the natural history of mitochondrial disease to inform the design and facilitate the conduction of clinical trials. It also serves as a catalyst for translating basic research results into clinical practice. The global mitochondrial registry and natural history study provides for all contingencies of national ethics and data protection rules including data access management. Currently participating networks are: - German network for mitochondrial diseases - mitoNET, Germany/Austria - Italian Registry of Mitochondrial Patients - Mitocon, Italy The inclusion of other networks and countries is possible and explicitly welcome. A major advantage of the global registry is that countries can join in, saving a lot of time, effort and funding. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05554835
Study type Observational [Patient Registry]
Source LMU Klinikum
Contact Boriana Büchner, Dr.
Phone +49 89 4400
Email boriana.buechner@med.uni-muenchen.de
Status Recruiting
Phase
Start date February 1, 2009
Completion date December 2040

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