Researchers launch study to unlock secrets of rare mitochondrial disorder
NCT ID NCT01532791
First seen Feb 01, 2026 · Last updated May 13, 2026 · Updated 12 times
Summary
This study aims to learn more about mitochondrial diseases caused by the m.3243A>G mutation, which can cause symptoms like migraines, seizures, hearing loss, and balance issues. Researchers will follow 300 participants, including mutation carriers and their maternal relatives, over time using brain scans, blood tests, and physical exams. No treatments are given; the goal is to better understand the disease to help develop future therapies.
Disclaimer
Read more
Show less
This is a summary of
the original study
.
Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for MELAS OR M.3243 A>G MITOCHONDRIAL DNA MUTATION CARRIER are added.
By submitting, you agree to our Terms of use
Contacts and locations
Show contact details
Enter your email to view the contact information for this study.
By submitting, you agree to our Terms of use
Study contacts
-
Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
-
Columbia University
RECRUITINGNew York, New York, 10032, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
Explore the condition pages connected to this study.