10,000 transplant patients and donors join long-term data study
NCT ID NCT01062581
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study creates a registry of up to 10,000 people who have received or donated an organ at the University of Minnesota. Researchers will collect and store health information to help answer future questions about transplants. No new treatments or procedures are being tested.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 10,000 people
The number the study aims to enrol. It can still change while the study runs.
- Start date
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Mar 1997
- Expected to finish
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Jan 2050
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
University of Minnesota Transplant Center University of Minnesota Medical Center, Fairview
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Received a transplanted organ at the University of Minnesota * Living donor who donates an organ at the University of Minnesota Exclusion Criteria: * Did not receive a transplant at the University of Minnesota * Did not donate an organ at the University of Minnesota
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University of Minnesota Transplant Information Services
RECRUITINGMinneapolis, Minnesota, 55414, United States
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Other studies related to the condition(s) this trial covers.
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