Global Registry and Natural History Study for Mitochondrial Disorders

Launched by LMU KLINIKUM · Sep 23, 2022

Keywords

ClinConnect Summary

The Global Registry and Natural History Study for Mitochondrial Disorders is a research project aimed at understanding various mitochondrial diseases, which are conditions that affect how our cells produce energy. The study will create a worldwide database to gather information from patients with these disorders, making it easier for researchers to learn more about their effects, measure health outcomes, and develop new treatments. This is a chance for patients from all walks of life to contribute to important research that can help improve understanding and care for these complex conditions.

To be eligible for this study, participants should either have a suspected or confirmed mitochondrial disease and be willing to take part in the research. Since the study is open to all ages and genders, many individuals and families may qualify. Participants can expect to share their experiences and health information, which will help researchers gain valuable insights into these diseases. This study is currently recruiting, so it’s a good opportunity for those interested in contributing to the advancement of knowledge in mitochondrial disorders.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • suspected or confirmed mitochondrial disease
• • willingness to participate
• Exclusion Criteria:
• • unwillingness to participate