Worldwide effort to track rare genetic obesity
NCT ID NCT07296900
First seen Jan 07, 2026 · Last updated May 05, 2026 · Updated 19 times
Summary
This study creates a global registry to collect health information from people with genetic obesity. Researchers aim to better understand how the condition progresses, what complications arise, and how different treatments work. The registry will include up to 5,000 participants from routine clinic visits, focusing on physical exams and lab tests.
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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.
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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Ulm University Clinic
RECRUITINGUlm, Germany
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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