10,000 transplant patients join landmark registry
NCT ID NCT01062581
First seen Apr 25, 2026 · Last updated May 20, 2026 · Updated 6 times
Summary
This study creates a registry to collect health information from up to 10,000 people who have received or donated an organ at the University of Minnesota. Researchers will track outcomes over time to better understand transplant success and donor health. No new treatments are being tested; the goal is to gather data for future research.
Disclaimer
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This is a summary of
the original study
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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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University of Minnesota Transplant Information Services
RECRUITINGMinneapolis, Minnesota, 55414, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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